ACHB Enterprise Co.

Listed in a source registry

Google Maps public business listing

Verified facts

• corporate-mail-on-domain (green), checked 2026-08-03 Mail server of the company domain
• domain-registered (green), checked 2026-08-03 Domain registry record
• sanctions-clear (green), checked 2026-08-03 OpenSanctions
• fda-registered (green), checked 2026-08-03 FDA
• fda-contract-manufacturer (green), checked 2026-08-03 FDA
• debarment-clear (green), checked 2026-08-03 OpenSanctions
• market-access-us (green), checked 2026-08-23 FDA device establishment registration (openFDA, U.S. Food and Drug Administration)
• 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)
• facility-registered (green), checked 2026-08-14 Taiwan Industrial Development Administration, registered factory directory (status: producing)
• registry-id-verified (green), checked 2026-08-14 Taiwan International Trade Administration, import/export firm registry (BOFT)
• export-registered (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

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)
• Machinery sold in the EU needs CE marking with a declaration of conformity under the EU machinery rules. European Commission

Check independently

• Sanctions and watchlists (OpenSanctions)