Medtronic
心臓血管、外科、糖尿病、神経科学の医療技術。
メドトロニックは、ダブリンの事業所で心臓血管、外科、糖尿病、神経科学の医療技術を製造しています。同社は、上場主要市場全体でヘルスケア システム、研究所、OEM パートナー、または規制対象の輸出顧客に供給しています。
- Type
- Manufacturer
- Location
- Dublin, Ireland
- Founded
- 1949
- Website
- medtronic.com
- Categories
- 医療およびヘルスケア用品, 家電
- Markets
- アイルランド, アメリカ合衆国, ドイツ, 日本
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)