Medtronic
Kardiyovasküler, cerrahi, diyabet ve sinirbilim tıp teknolojileri.
Medtronic, Dublin operasyonlarından kardiyovasküler, cerrahi, diyabet ve sinir bilimi tıbbi teknolojileri üretmektedir. Şirket, listelenen birincil pazarlarda sağlık sistemleri, laboratuvarlar, OEM ortakları veya düzenlemeye tabi ihracat müşterilerine hizmet vermektedir.
- Type
- Manufacturer
- Location
- Dublin, Ireland
- Founded
- 1949
- Website
- medtronic.com
- Categories
- Tıbbi ve Sağlık Malzemeleri, Tüketici Elektroniği
- Markets
- İrlanda, Amerika Birleşik Devletleri, Almanya, Japonya
Verified facts
- domain-registered (green), checked 2026-08-09 Domain registry record
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- fda-registered (green), checked 2026-08-09 FDA
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
Claimed certifications
- ISO 13485, Medical Devices Quality IAF CertSearch
- FDA Registered FDA Establishment Registration
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)
- Electronics for the EU need CE marking incl. RoHS substance limits, and producers must register for WEEE take-back in each member state of sale. European Commission (CE)
- Electronics for the US market need FCC equipment authorization under 47 CFR Part 15, which covers unintentional radiators such as switch-mode power supplies, not only radio devices. US FCC (Part 15)