Taiwan FDA registration 6af1bbb876facfdb2608365737d314bb
“Endo-Upex” Biopsy Forceps
TW: “安朵優倍斯”活體組織夾
Taiwan·Risk Class 2·MD·UPEX-MED CO., LTD.·Registered Dec 30, 2021 – Dec 30, 2026ActiveRegistration details
- Analysis ID
- 6af1bbb876facfdb2608365737d314bb
- License Form
- Ministry of Health Medical Device Import No. 035160
- Customs Code
- DHA05603516005
Company information
- Manufacturer
- UPEX-MED CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- MedPower Medical Co., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H1075 Gastroenterology - Urology biopsy instruments
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 30, 2021
- Expiry Date
- Dec 30, 2026
About this record
Access comprehensive regulatory information for “Endo-Upex” Biopsy Forceps in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6af1bbb876facfdb2608365737d314bb and manufactured by UPEX-MED CO., LTD.. The authorized representative in Taiwan is MedPower Medical Co., LTD..
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