Medtronic plc

Medtronic plc

MDT

$87.96

Updated: 25/09/2026, 16:26:18

Market Cap
$112.55B
Sector
Healthcare
Industry
Medical - Devices
Country
IE
Stock valuation chart
One-year closing share-price history for MDT
Company Profile

Medtronic plc is a leading global medical technology enterprise that invents, develops, manufactures, and distributes an extensive range of device-based medical therapies. These solutions serve healthcare systems, clinicians, physicians, and patients across the world. The company's operations are categorized into several key portfolios: Cardiovascular Portfolio: This segment focuses on cardiac health, providing technologies for heart rhythm management, including implantable pacemakers, defibrillators, and monitoring systems, alongside cardiac ablation tools and remote patient software. It also addresses structural heart issues with products like aortic and pulmonary valves, surgical repair devices, and endovascular stent grafts, in addition to offerings for percutaneous coronary interventions (e.g., angioplasty balloons). Medical Surgical Portfolio: Offering a broad spectrum of surgical instruments and therapies, this division includes staples, vessel sealing devices, wound closure products, and electrosurgical equipment. It also pioneers surgical artificial intelligence and robotic-assisted platforms, alongside solutions for hernia repair, gynecology, lung conditions, minimally invasive gastrointestinal and hepatologic diagnostics, patient monitoring, airway management, ventilation therapies, and renal disease. Neuroscience Portfolio: This division delivers specialized products for a diverse group of medical professionals, such as spinal surgeons, neurosurgeons, neurologists, pain management specialists, and ENT experts. Its offerings span energy surgical instruments, advanced image-guided and intra-operative imaging systems, robotic guidance for spine procedures, and therapies targeting the brain's vasculature. Diabetes Operating Unit: Dedicated to diabetes management, this unit provides innovative solutions like insulin pumps and their associated consumables, continuous glucose monitoring (CGM) systems, and smart insulin pen technologies. Established in 1949, Medtronic plc maintains its corporate headquarters in Dublin, Ireland.

USD
NYSE
CEO: Geoffrey Straub Martha
Employees: 95,000
https://www.medtronic.com
Asset Summaries
Latest generated summaries for MDT

No summaries found.

Detailed business
Evidence-backed facts extracted from the latest official annual filing.
MDT-10-k-fy2026.html3.6 MBtext/htmlENFiled 18/06/2026Period ended 24/04/2026

Business monitoring

Reported and calculated KPIs plus operational exposure disclosed in the FY 2026 filing.

Evidence-backed · 62 KPI observations

Revenue

$36.4B

FY 2026 · Reported

Net income

$4.8B

FY 2026 · Reported

Gross margin

65.0%

FY 2026 · Calculated

Free cash flow

$5.4B

FY 2026 · Calculated

R&D intensity

N/A

FY — · Reported

Share repurchases

$1.0B

FY 2026 · Reported

Earnings and cash generation
USD billions, directly sourced from inline XBRL; free cash flow is operating cash flow less capex.
Profitability and reinvestment
Margins and R&D as a percentage of revenue.
Top products and services
Products and services mentioned in the filing; a quantitative sales breakdown was not disclosed.

Other offerings mentioned without separate sales

Cardiac Rhythm & Heart Failure products
Pulsed field ablation portfolio
Leadless pacing — Micra
Insertable cardiac monitoring — LINQ II

Area-level product sales are displayed only when the filing reports a product × geography breakdown. Regional totals are not allocated across products by estimation.

Geographic footprint
What the filing identifies, separated by location role so partner manufacturing is not presented as Apple-owned factories.
1 named headquarters
0 manufacturing countries
0 individually named factories

Map layer

Pins show disclosed operations. The heatmap colors the filing’s reported geographies; regional figures shade the region and are not estimates for each country.

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Named headquarters Manufacturing partner country

Only locations and quantities explicitly supported by the filing are displayed. A country-level manufacturing percentage or product allocation is shown only when the source discloses it; materiality scores are never presented as production shares.

How the business makes money

Company overview

Medtronic plc, headquartered in Galway, Ireland, is the leading global healthcare technology company, serving healthcare systems, physicians, clinicians, and patients in more than 150 countries.

98%
Source evidence
“Medtronic plc, headquartered in Galway, Ireland, is the leading global healthcare technology company. Medtronic was founded in 1949 and today serves healthcare systems, physicians, clinicians, and patients in more than 150 countries worldwide.”

Diabetes exits reportable segments

Diabetes no longer a reportable segment starting Q4 FY2026; Diabetes net sales $3,112M in FY2026

98%
Source evidence
“Starting in the fourth quarter of fiscal year 2026, the Diabetes Business is no longer considered a reportable segment. Prior period net sales have been recast to conform to the new presentation.”

Cardiovascular Portfolio structure

Cardiovascular Portfolio comprises Cardiac Rhythm & Heart Failure, Structural Heart & Aortic, and Coronary & Peripheral Vascular divisions.

97%
Source evidence
“The Cardiovascular Portfolio is made up of the Cardiac Rhythm & Heart Failure, Structural Heart & Aortic, and Coronary & Peripheral Vascular divisions.”

Reportable segments

Three reportable segments: Cardiovascular, Neuroscience, Medical Surgical; Diabetes removed from segments in Q4 FY2026 after MiniMed IPO.

97%
Source evidence
“We have three reportable segments that primarily develop, manufacture, distribute, and sell device-based medical therapies and services: the Cardiovascular Portfolio, the Neuroscience Portfolio, and the Medical Surgical Portfolio.”

Reportable segments

Reportable segments are Cardiovascular, Neuroscience, and Medical Surgical; Diabetes was removed as a reportable segment in Q4 FY2026

95%
Source evidence
“Starting in the fourth quarter of fiscal year 2026, the Diabetes Business is no longer considered a reportable segment. Prior period net sales have been recast to conform to the new presentation.”

Primary customers

Healthcare systems, clinics, third-party providers, distributors, government programs, GPOs

96%
Source evidence
“The Company's primary customers include healthcare systems, clinics, third-party healthcare providers, distributors, and other institutions, including governmental healthcare programs and group purchasing organizations.”

Cardiovascular customer specialists

Cardiovascular products are used by electrophysiologists, implanting cardiologists, heart failure specialists, cardiovascular/cardiothoracic/vascular surgeons, and interventional cardiologists and radiologists.

95%
Source evidence
“The primary medical specialists who use our Cardiovascular products include electrophysiologists, implanting cardiologists, heart failure specialists, cardiovascular, cardiothoracic, and vascular surgeons, and interventional cardiologists and radiologists.”

Cardiac Rhythm & Heart Failure products

CRHF division offers pacemakers (incl. Micra leadless), ICDs, CRT devices, pulsed-field and cryoablation EP solutions, and insertable cardiac monitors (LINQ II with AccuRhythm AI).

96%
Source evidence
“The division develops, manufactures, and markets products for the diagnosis, treatment, and management of heart rhythm disorders and heart failure.”

Pulsed field ablation portfolio

Cardiac ablation suite includes PulseSelect and Affera Sphere-360 single-shot pulsed field ablation catheters, Affera Sphere-9 focal catheter, Affera mapping system, and Arctic Front cryoablation.

96%
Source evidence
“The portfolio includes the PulseSelect and Affera Sphere-360 single shot pulsed field ablation catheters, the Affera Sphere-9 focal catheter, providing high density mapping capabilities combined with dual radio frequency and pulsed field energies.”

Leadless pacing — Micra

Micra transcatheter pacing system (Micra VR and Micra AV) is leadless and treats patients with atrioventricular block.

95%
Source evidence
“The Micra transcatheter pacing system, which is leadless and does not have a subcutaneous device pocket like a conventional pacemaker, includes the Micra VR and the Micra AV device families.”

Insertable cardiac monitoring — LINQ II

Reveal LINQ and LINQ II insertable cardiac monitors serve cryptogenic stroke and transient-symptom patients; AccuRhythm AI reduces clinic workload; LINQ II offers extended longevity and remote programming.

94%
Source evidence
“LINQ II, the premium portfolio device, offers extended device longevity and remote programming capab”

U.S. vs international net sales FY2026

U.S. $18,103M vs International $18,261M in FY2026

97%
Source evidence
“Total net sales$18,103 $17,171 $16,562 $18,261 $16,365 $15,802”

Net sales by segment FY2026/2025/2024

Total net sales $36,364M (FY2026), $33,537M (FY2025), $32,364M (FY2024); largest segment Cardiovascular $13,976M FY2026

98%
Source evidence
“Cardiac Rhythm & Heart Failure$7,504 $6,392 $5,995 ... Total net sales$36,364 $33,537 $32,364”

Net sales by segment and division FY2026 vs FY2025

Total net sales $36,364M FY2026 vs $33,537M FY2025 (+8%); Cardiovascular $13,976M (+12%), Neuroscience $10,287M (+4%), Medical Surgical $8,815M (+5%), Diabetes $3,112M (+13%) (in millions)

98%
Source evidence
“Cardiac Rhythm & Heart Failure$7,504 $6,392 17 %”

Operations and dependencies

Petroleum-based materials, resins, pulp; oil/gas cost exposure

Uses resins, petroleum-based materials and pulp; oil and gas prices significantly affect freight and utility costs; commodity prices and tariffs could impact supply

95%
Source evidence
“We use resins, other petroleum-based materials and pulp as raw materials in some of our products, and the prices of oil and gas also significantly affect our costs for freight and utilities.”

Currency transaction losses

Currency transaction losses: $57M (FY2026), $309M (FY2025), $123M (FY2024)

93%
Source evidence
“Currency transaction losses for fiscal years 2026, 2025, and 2024 were $57 million, $309 million, and $123 million, respectively.”

Puerto Rico key manufacturing site

Puerto Rico subsidiary operates one of Medtronic's key manufacturing sites

92%
Source evidence
“the allocation of income between Medtronic, Inc. and its wholly-owned subsidiary operating in Puerto Rico, which operates one of our key manufacturing sites”

Sole-source suppliers and prior semiconductor/resin shortages

Sole-source supplier dependencies; prior global shortages of semiconductors and resins disrupted manufacturing supply chain

97%
Source evidence
“global shortages of certain components such as semiconductors and resins have previously caused, and may in the future cause, disruptions to our product manufacturing supply chain.”

Positioning and strategy

BlueSync remote monitoring technology

Azure pacemakers feature Medtronic-exclusive BlueSync technology enabling automatic wireless remote monitoring with increased device longevity.

93%
Source evidence
“Azure pacemakers feature Medtronic-exclusive BlueSync technology, which enables automatic, secure wireless remote monitoring with increased device longevity.”

Diabetes separation / MiniMed IPO

In May 2025 Medtronic announced intent to separate its Diabetes Business into MiniMed Group, Inc.; MiniMed completed an IPO on March 9, 2026, and Diabetes ceased to be a reportable segment in Q4 FY2026.

97%
Source evidence
“In May 2025, the Company announced its intent to separate the Diabetes Business, with the intention to create a new independent, publicly traded company, MiniMed Group, Inc. (MiniMed). On March 9, 2026, MiniMed completed an initial public offering (the IPO).”

Global market presence

Serves healthcare systems, physicians, clinicians, and patients in more than 150 countries; mission written by founder in 1960.

95%
Source evidence
“we use our local presence and scale to increase the adoption of our products and services in markets around the globe”

Strategy: accelerate innovation-driven growth

Accelerate innovation-driven growth via product launches, pipeline, and local presence/scale to increase global adoption.

95%
Source evidence
“Accelerate innovation-driven growth: The combination of our attractive end markets, recent product launches and robust pipeline is expected to enable continued strong revenue growth.”

Strategy: data, AI, and automation

Turn data, AI, and automation into action: real-time tailored therapies, remote monitoring, new standards of care.

95%
Source evidence
“Turn data, AI, and automation into action: We are confident in our ability to maximize new technology, AI, and data and analytics to tailor therapies in real-time, facilitating remote monitoring and care delivery.”

Reliance on investments and investment collaborations for new technologies

Strategy includes acquisitions, divestitures, and third-party R&D funding arrangements; relies on investments and collaborations to access new technologies

93%
Source evidence
“historically we have relied, and expect to continue to rely, upon investments and investment collaborations to provide us access to new technologies both in areas served by our existing businesses as well as in new areas.”

Risks, financing, and outlook

Diabetes Business separation

Diabetes Business separation is impending; starting Q4 FY2026 Diabetes is no longer a reportable segment and prior period net sales were recast

95%
Source evidence
“Starting in the fourth quarter of fiscal year 2026, the Diabetes Business is no longer considered a reportable segment.”

Estimated FY2027 net tariff impact

Estimated pre-tax net tariff impact of $250 million in fiscal year 2027, excluding government refunds

95%
Source evidence
“Based on current rates as of June 3, 2026, we estimate the pre-tax net tariff impact to be $250 million in fiscal year 2027, excluding any considerations of government refunds.”

Non-GAAP adjustments composition

FY2026 non-GAAP adjustments include $1,772M intangible amortization (incl. $121M accelerated Cardiovascular amortization), $370M restructuring, $113M litigation charges

95%
Source evidence
“The Company recognized $121 million and $151 million of accelerated amortization on certain intangible assets within the Cardiovascular Portfolio for fiscal years 2026 and 2025, respectively.”

Supreme Court IEEPA tariff ruling and CBP refund process

On February 20, 2026, the U.S. Supreme Court ruled IEEPA tariff policies unconstitutional; CBP launched an IEEPA tariff refund request portal on April 20, 2026

90%
Source evidence
“On February 20, 2026, the U.S. Supreme Court ruled that President Trump's tariff policies under the International Emergency Economic Powers Act ("IEEPA") are unconstitutional.”

FY2026 certain tax adjustments

FY2026 net tax charges of $260 million primarily from intercompany IP sale and Diabetes separation, partially offset by uncertain tax position interest benefit

90%
Source evidence
“The net charges for fiscal year 2026 primarily relates to the impact of an intercompany sale of intellectual property, the net tax charge as a result of the separation of the Diabetes Business”

E.U. medical device regulation costs (FY2025)

FY2025 included $52 million of charges for incremental compliance costs with new E.U. medical device regulations, treated as one-time/duplicative

90%
Source evidence
“The charges represent incremental costs of complying with the new European Union (E.U.) medical device regulations for previously registered products”

EU MDR transition deadlines

EU MDR effective May 26, 2021; implementation extended to end-2027 for high-risk devices and end-2028 for medium/low-risk devices

97%
Source evidence
“The European Commission extended the implementation period to the end of 2027 for high-risk devices and to the end of 2028 for medium and low risk devices.”

Data privacy regimes: HIPAA, HITECH, GDPR, UK privacy, China PIPL

Subject to HIPAA, HITECH, state privacy laws, GDPR, UK privacy laws, and China's PIPL; compliance may require significant additional cost

96%
Source evidence
“such as the General Data Protection Regulation (GDPR) in the European Economic Area, the United Kingdom’s privacy laws, and China's Personal Information Protection Law (PIPL).”

Reimbursement regulation and Sunshine Act

Reimbursement subject to HHS/Medicare/Medicaid regulation; Sunshine Act (Open Payments) annual payment transparency reporting; coverage changes could reduce demand and prices

95%
Source evidence
“we are subject to the U.S. Physician Payments Sunshine Act (Open Payments), which requires us to annually report certain payments and other transfers of value we make to U.S.-licensed physicians, certain allied health professionals, and U.S. teaching hospitals.”

Anti-corruption laws exposure

FCPA, U.K. Bribery Act, Irish anti-corruption law exposure via government customers

94%
Source evidence
“many of our customer relationships outside of the U.S. are with governmental entities and are therefore potentially subject to such laws”

US FDA workforce reductions impacting approval timelines

FDA workforce reductions/reorganization have impacted and could continue to impact product approval timelines; HHS changes could affect reimbursement

94%
Source evidence
“workforce reductions and agency reorganization at the U.S. FDA have, and could continue to have, an impact on product approval timelines and other types of agency oversight.”

EU AI Act and evolving AI regulation

EU AI Act and evolving global AI regulation may impact business; compliance may require significant expenditures or limit AI use

94%
Source evidence
“including the EU AI Act, which may impact our business.”

Global competition across 150+ countries

Competes in therapeutic and diagnostic markets in 150+ countries; faces competitors from large firms to niche makers and GLP-1 pharma alternatives

98%
Source evidence
“We compete in both the therapeutic and diagnostic medical markets in more than 150 countries throughout the world.”

China volume-based procurement pricing pressure

Government-driven procurement including China volume-based procurement may require price concessions and constrain non-price competition; clawback risk

96%
Source evidence
“national and provincial tender pricing programs such as volume‑based procurement initiatives in China, may require significant price concessions and constrain our ability to compete on factors other than price.”

Sterilization capacity concentration

Key products sterilized at particular facilities with constrained capacity and limited alternate options; EtO and PFAS regulations may add constraints

95%
Source evidence
“several of our key products are manufactured or sterilized at a particular facility, with constrained capacity and limited options for alternate sterilization facilities.”

Trade regulations, tariffs, and sanctions exposure

Extensive trade regulation exposure including tariffs, export controls, sanctions, and anti-boycott laws; non-compliance could disrupt sales and distribution

94%
Source evidence
“The movement of products, services, technology, know-how, and investment across borders subjects us to extensive trade laws and regulations, including tariff regulations adopted by different countries or trading zones.”

AI execution and adoption risk

Must integrate/scale AI and digital technologies across products and operations at pace with competitors or risk reduced competitiveness and market share loss

94%
Source evidence
“If we are unable to effectively integrate, scale, or apply AI and digital technologies across our products and operations at a pace comparable to competitors or new market entrants, we could experience reduced competitiveness, slower growth, or loss of market share.”

Cybersecurity/ransomware risk

Ransomware and cyber-attack risk across own and third-party systems; AI amplifies threats

94%
Source evidence
“One of the most prevalent attacks on large organizations has been ransomware, which can have a devastating impact on an organization’s operations.”

AI-related business and regulatory risk

AI systems risks: flaws, biases, malfunctions, emerging regulation penalties

92%
Source evidence
“These systems are susceptible to flaws, biases, malfunctions or manipulations, which may disrupt our operations, result in erroneous decision-making, elevate our cyber risk profile, or expose us to penalties from non-compliance with emerging regulations.”

Macroeconomic and geopolitical risk factors

Management cites pricing pressure, trade policy, currency, inflation, rates, reimbursement challenges, China tender pricing, registration delays, and supply chain challenges as potential negative factors

90%
Source evidence
“national and provincial tender pricing for certain products, particularly in China, replacement cycle challenges, and supply chain challenges from time to time.”

Material exposure graph

United States
Revenue Exposure

U.S. (incl. territories) generated $18,103M of FY2026 net sales, roughly half of worldwide revenue.

Relevance 90·Dependency 85·Confidence 96
Source evidence
“The U.S. revenue includes United States and U.S. territories ... Total net sales$18,103”
Healthcare systems, clinics, distributors, GPOs, government programs
Revenue Exposure

Revenue principally derived from device-based therapies sold to healthcare systems, clinics, third-party providers, distributors, governmental programs and GPOs.

Relevance 90·Dependency 85·Confidence 96
Source evidence
“The Company's revenues are principally derived from device-based medical therapies and services ... The Company's primary customers include healthcare systems, clinics, third-party healthcare providers, distributors, and other institutions”
U.S. FDA
Regulatory Exposure

FDA approval (510(k), PMA) and inspections govern product commercialization; FDA workforce reductions have impacted approval timelines and oversight.

Relevance 85·Dependency 70·Confidence 96
Source evidence
“workforce reductions and agency reorganization at the U.S. FDA have, and could continue to have, an impact on product approval timelines”
tariffs
Cost Driver

U.S., China, and other jurisdictions' tariffs are expected to add an estimated $250 million pre-tax net cost in FY2027; further escalation could have a material adverse effect.

Relevance 85·Dependency 60·Confidence 95
Source evidence
“Further escalation or expansion of trade barriers could have a material adverse effect on our results of operations.”
EU Medical Device Regulation (EU MDR)
Regulatory Exposure

EU MDR imposes significant additional pre-market and post-market requirements; transition deadlines end-2027 (high-risk) and end-2028 (medium/low-risk).

Relevance 82·Dependency 65·Confidence 96
Source evidence
“it imposes significant additional pre-market and post-market requirements (EU MDR)”
Cardiac specialists (electrophysiologists, cardiologists, surgeons)
Customer Exposure

Cardiovascular product demand flows through specialist physicians who implant and use Medtronic devices.

Relevance 80·Dependency 75·Confidence 95
Source evidence
“The primary medical specialists who use our Cardiovascular products include electrophysiologists, implanting cardiologists, heart failure specialists, cardiovascular, cardiothoracic, and vascular surgeons, and interventional cardiologists and radiologists.”
United States
Legal Exposure

IRS transfer-pricing litigation over Puerto Rico income allocation could materially affect financial condition if adverse.

Relevance 80·Dependency 40·Confidence 95
Source evidence
“The outcome of Medtronic, Inc.'s U.S. tax litigation could have a material adverse impact on our financial condition.”
semiconductors
Supplier Dependency

Global semiconductor shortages have previously disrupted Medtronic's product manufacturing supply chain and may recur.

Relevance 78·Dependency 55·Confidence 95
Source evidence
“global shortages of certain components such as semiconductors and resins have previously caused, and may in the future cause, disruptions to our product manufacturing supply chain.”
AI and data analytics
Technology Dependency

Strategic pillar relies on AI and data analytics for real-time therapy tailoring and remote monitoring; AccuRhythm AI differentiates LINQ II monitors.

Relevance 75·Dependency 60·Confidence 92
Source evidence
“Turn data, AI, and automation into action: We are confident in our ability to maximize new technology, AI, and data and analytics to tailor therapies in real-time”
artificial intelligence
Technology Dependency

AI, machine learning and data science impact Medtronic products, operations, and the competitive landscape; failure to scale AI at competitor pace risks market share loss.

Relevance 75·Dependency 50·Confidence 93
Source evidence
“data science, machine learning and AI are all impacting our products and operations and the competitive landscape in which we operate”
China
Revenue Exposure

China volume-based procurement and tender pricing programs may force price concessions and clawbacks, adversely affecting revenue and margins in that market.

Relevance 72·Dependency 45·Confidence 94
Source evidence
“national and provincial tender pricing programs such as volume‑based procurement initiatives in China, may require significant price concessions”
AI-enabled device differentiation
Competitive Exposure

Exclusive BlueSync wireless and AccuRhythm AI features are cited as differentiators vs. conventional devices.

Relevance 70·Dependency 55·Confidence 90
Source evidence
“Both portfolio devices have unmatched accuracy and a streamlined workflow with AccuRhythm AI algorithms to reduce clinic workload and data burden.”
OECD Pillar Two Model Rules
Regulatory Exposure

15% global minimum tax applies to Medtronic from FY2025, including via Irish enactment.

Relevance 65·Dependency 35·Confidence 93
Source evidence
“A number of countries, including Ireland, have enacted legislation to implement the core elements of the Pillar Two Model Rules, which were effective for Medtronic in fiscal year 2025.”
EU AI Act
Regulatory Exposure

EU AI Act and evolving global AI regulation may impact Medtronic's use of AI in products and operations and compliance may require significant expenditures.

Relevance 62·Dependency 40·Confidence 92
Source evidence
“including the EU AI Act, which may impact our business.”
Puerto Rico manufacturing site
Raw Material Dependency

Key Puerto Rico manufacturing site underpins tax dispute; outcome could materially affect results.

Relevance 60·Dependency 50·Confidence 90
Source evidence
“its wholly-owned subsidiary operating in Puerto Rico, which operates one of our key manufacturing sites”
oil and gas prices
Commodity Exposure

Resins and petroleum-based materials are inputs, and oil/gas prices significantly affect freight and utility costs.

Relevance 60·Dependency 40·Confidence 93
Source evidence
“the prices of oil and gas also significantly affect our costs for freight and utilities.”
Diabetes Business
Revenue Exposure

Diabetes contributed $3,112M of FY2026 net sales ($2,178M international, $934M U.S.) but was removed from reportable segments in Q4 FY2026, consistent with a planned separation/divestiture path referenced by recast reporting.

Relevance 55·Dependency 35·Confidence 94
Source evidence
“Starting in the fourth quarter of fiscal year 2026, the Diabetes Business is no longer considered a reportable segment.”
Italy
Tax Exposure

Italian payback mechanism produced $90M incremental accrual in FY2025 and $39M reversal in FY2026, recorded as adjustments to net sales.

Relevance 55·Dependency 30·Confidence 95
Source evidence
“the incremental Italian payback accruals resulting from the two July 22, 2024 rulings by the Constitutional Court of Italy relating to certain prior years since 2015”
U.S. FCPA / anti-corruption laws
Regulatory Exposure

Government-administered healthcare systems abroad expose Medtronic to FCPA, U.K. Bribery Act and Irish anti-corruption law enforcement risk.

Relevance 55·Dependency 25·Confidence 92
Source evidence
“Because of the predominance of government-administered healthcare systems in many jurisdictions around the world, many of our customer relationships outside of the U.S. are with governmental entities and are therefore potentially subject to such laws.”
Full company information
Latest profile, trading, valuation, and identifier data stored for MDT.
Share price
$87.96
Market cap
$112.55B
Exchange
NYSE
Currency
USD
CEO
Geoffrey Straub Martha
Employees
95,000
IPO date
02/05/1973
Beta
0.574
Last dividend
$0.00
Day range
$87.12 – $88.53
52-week range
$73.31 – $106.33
1-day performance
-0.62%
1-year performance
19.98%
Current drawdown (1Y)
-17.28%
CIK
0001613103
CUSIP
G5960L103
ISIN
IE00BTN1Y115
Created
07/12/2025, 05:12:15
Last update
25/09/2026, 16:26:18

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