PART PRECISION SWEDEN AB

Listed in a source registry

US FDA device registration and listing (open.fda.gov)

Verified facts

• sanctions-clear (green), checked 2026-08-15 OpenSanctions
• fda-registered (green), checked 2026-08-15 FDA
• fda-contract-manufacturer (green), checked 2026-08-15 FDA
• debarment-clear (green), checked 2026-08-15 OpenSanctions
• facility-registered (green), checked 2026-08-07 US FDA device establishment registration (openFDA)
• registered-address (green), checked 2026-08-19 Bolagsverket, vardefulla datamangder (bulkfil)
• registered-manufacturer (green), checked 2026-08-19 Statistikmyndigheten SCB via Bolagsverket, vardefulla datamangder
• registry-id-verified (green), checked 2026-08-19 Bolagsverket, vardefulla datamangder (bulkfil)

Claimed certifications

• 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)

Check independently

• Sanctions and watchlists (OpenSanctions)