ACHB Enterprise Co.
ACHB चिकित्सा उपकरणों, जीवन विज्ञान उपकरणों और रोबोटिक्स के लिए OEM और ODM सटीक विनिर्माण प्रदान करता है। आईएसओ 13485, आईएसओ 9001, और आईएसओ
ACHB चिकित्सा उपकरणों, जीवन विज्ञान उपकरणों और रोबोटिक्स के लिए OEM और ODM सटीक विनिर्माण प्रदान करता है। आईएसओ 13485, आईएसओ 9001, और आईएसओ 14001 प्रमाणित।
- Type
- brand seeking distribution
- Location
- Tainan City, Taiwan
- Website
- https://www.achb-tw.com/
- Categories
- चिकित्सा एवं स्वास्थ्य देखभाल आपूर्तियाँ, औद्योगिक स्वचालन और रोबोटिक्स
Listed in a source registry
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