Taiwan FDA registration a81a39795499c11ad0be0f53947d8078
“CryoLife” PhotoFix Bovine Pericardial Patch
TW: “克優萊”弗特克斯牛心包嵌片
Taiwan·Risk Class 2·MD·CRYOLIFE INC·Registered Dec 22, 2020 – Dec 22, 2025ExpiredRegistration details
- Analysis ID
- a81a39795499c11ad0be0f53947d8078
- License Form
- Ministry of Health Medical Device Import No. 034227
- Customs Code
- DHA05603422706
Company information
- Manufacturer
- CRYOLIFE INC
- Manufacturer Country
- United States
- Authorized Representative
- EMERGO TAIWAN LIMITED
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)
- E3470 polypropylene
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 22, 2020
- Expiry Date
- Dec 22, 2025
About this record
Access comprehensive regulatory information for “CryoLife” PhotoFix Bovine Pericardial Patch in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a81a39795499c11ad0be0f53947d8078 and manufactured by CRYOLIFE INC. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices