Sanmina-SCI Systems Singapore Pte. Ltd.
- Type
- Manufacturer
- Location
- SINGAPORE North East, Singapore
- Founded
- 1983
- Categories
- Medical & Healthcare Supplies
Listed in a source registry
Verified facts
- debarment-clear (green), checked 2026-08-24 OpenSanctions
- fda-registered (green), checked 2026-08-24 FDA
- fda-contract-manufacturer (green), checked 2026-08-24 FDA
- sanctions-clear (green), checked 2026-08-24 OpenSanctions
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- facility-registered (green), checked 2026-08-07 US FDA device establishment registration (openFDA)
- registered-manufacturer (green), checked 1983-11-11 ACRA Information on Corporate Entities (data.gov.sg)
- registered-since (green), checked 1983-11-11 ACRA Information on Corporate Entities (data.gov.sg)
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)