Taiwan FDA registration 2de412651294347d1a9ee9ea42be262f
“BIOVER” Microvascular Clamps
TW: “畢歐芙”顯微血管夾
Taiwan·Risk Class 2·MD·BIOVER AG·Registered Jan 29, 2018 – Jan 29, 2028ActiveRegistration details
- Analysis ID
- 2de412651294347d1a9ee9ea42be262f
- License Form
- Ministry of Health Medical Device Import No. 030717
- Customs Code
- DHA05603071703
Company information
- Manufacturer
- BIOVER AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E4450 Vascular Clip
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 29, 2018
- Expiry Date
- Jan 29, 2028
About this record
Access comprehensive regulatory information for “BIOVER” Microvascular Clamps in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2de412651294347d1a9ee9ea42be262f and manufactured by BIOVER AG. The authorized representative in Taiwan is GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH.
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