Shummi Enterprise Co., Ltd.
Vật tư và thiết bị nha khoa, Đài Loan
Shummi Enterprise Co., Ltd. là công ty trong lĩnh vực Vật tư và thiết bị nha khoa tại Taipei, Đài Loan. Được đăng ký trong cơ quan đăng ký doanh nghiệp công.
- Type
- brand seeking distribution
- Location
- Taipei, Taiwan
- Categories
- Vật tư và thiết bị nha khoa, Vật tư y tế và chăm sóc sức khỏe
Listed in a source registry
Verified facts
- export-registered (green), checked 2026-08-07 US FDA device establishment registration (openFDA)
- registry-active-global (green), checked 2026-08-20 Taiwan Ministry of Economic Affairs, Commerce Development Administration (經濟部商業發展署), company registration open data (GCIS)
- registry-change-published (green), checked 2026-08-20 Taiwan Ministry of Economic Affairs, Commerce Development Administration (經濟部商業發展署), company registration open data (GCIS)
- officer-appointed (green), checked 2026-08-20 Taiwan Ministry of Economic Affairs, Commerce Development Administration (經濟部商業發展署), company registration open data (GCIS)
- registered-trade-only (amber), checked 2026-08-20 Taiwan Ministry of Economic Affairs, Commerce Development Administration (經濟部商業發展署), company registration open data (GCIS)
- ownership-on-record (green), checked 2026-08-20 Taiwan Ministry of Economic Affairs, Commerce Development Administration (經濟部商業發展署), company registration open data (GCIS)
- facility-registered (green), checked 2026-08-07 US FDA device establishment registration (openFDA)
- sanctions-clear (green), checked 2026-09-02 OpenSanctions
- fda-registered (green), checked 2026-09-02 FDA
- fda-contract-manufacturer (green), checked 2026-09-02 FDA
- debarment-clear (green), checked 2026-09-02 OpenSanctions
- registry-id-verified (green), checked 2026-08-14 Taiwan International Trade Administration, import/export firm registry (BOFT)
- registry-activity (green), checked 2026-08-14 Taiwan Ministry of Finance, national business tax 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)