Medtronic, Inc.

Manufacturer of medical devices registered in the European database in Minneapolis, United States.

Registration number (SRN)	`US-MF-000019977`
Role	Manufacturer
Status	Active
Country	United States
City	MN 55432 Minneapolis
Address	Medtronic Parkway, 710 MN 55432 Minneapolis
Registered on	2022-02-07

United States market access

FDA establishment register	Registered with the U.S. FDA
Matched entry	Medtronic, Inc. (US) · FDA 3004185781

Notified body certificates

Certificate	Status	Expiry	Type	Body
`MDR 731886`	reissued	2031-08-25	Technical documentation	NB 2797
`MDR 731827`	reissued	2031-08-25	Quality management system	NB 2797
`MDR 730924`	reissued	2031-07-19	Technical documentation	NB 2797
`MDR 730827`	reissued	2031-07-19	Quality management system	NB 2797
`G70 039709 1509`	supplemented	2028-12-27	Technical documentation	NB 0123
`G70 039709 1443`	supplemented	2028-08-13	Technical documentation	NB 0123
`G70 039709 1408`	valid	2027-11-17	Technical documentation	NB 0123
`G70 039709 1366`	reissued	2031-09-07	Technical documentation	NB 0123
`G70 039709 1362`	reissued	2031-09-01	Technical documentation	NB 0123
`G70 039709 1361`	reissued	2031-09-09	Technical documentation	NB 0123
`G70 039709 1296`	supplemented	2030-07-02	Technical documentation	NB 0123
`G15 039709 1576`	valid	2031-07-28	Quality management system	NB 0123
`G15 039709 1560`	reissued	2030-07-02	Quality management system	NB 0123
`G10 039709 1477`	valid	2028-06-01	Quality management system	NB 0123
`G10 039709 1455`	valid	expires 2026-11-30 — 46 days	Quality management system	NB 0123
`2266041TD02`	supplemented	2029-12-01	Technical documentation	NB 0344
`1000277712`	valid	2031-06-08	Technical documentation	NB 0297
`1000225868`	valid	2031-06-08	Quality management system	NB 0297

⚠️ State of the register on 2026-08-20. EUDAMED shows only the current version of a certificate — earlier versions are not published, by the Commission or by anyone. A certificate shown as valid here may have changed since. For a legally binding check, consult EUDAMED directly.

The SRN is the registration number assigned by the European Commission. It has been mandatory since 28 May 2026 for any operator placing a medical device on the Union market. Contact details are published in the official register; we do not reproduce them here.

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