Taiwan FDA registration 972c2a50b5987307afe31abd2e9a1bcd
“Applied”GelPOINT V-Path Transvaginal Access Platform
TW: “安培”經陰道手術通路
Taiwan·Risk Class 2·MD·APPLIED MEDICAL RESOURCES CORPORATION·Registered Aug 25, 2022 – Aug 25, 2027ActiveRegistration details
- Analysis ID
- 972c2a50b5987307afe31abd2e9a1bcd
- License Form
- Ministry of Health Medical Device Import No. 035768
- Customs Code
- DHA05603576806
Company information
- Manufacturer
- APPLIED MEDICAL RESOURCES CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- DOUBLE-SUCCESS CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- l Obstetrics and Gynecology
- Product Type (Level 2)
- L1640 recessed mirror and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 25, 2022
- Expiry Date
- Aug 25, 2027
About this record
Access comprehensive regulatory information for “Applied”GelPOINT V-Path Transvaginal Access Platform in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 972c2a50b5987307afe31abd2e9a1bcd and manufactured by APPLIED MEDICAL RESOURCES CORPORATION. The authorized representative in Taiwan is DOUBLE-SUCCESS CO., LTD..
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