Taiwan FDA registration 03e52e70f3bfa7efef60fe23e6b43f05
“Cytoplast” PTFE Suture
TW: “山多普斯”非吸收聚四氟乙烯縫合線
Taiwan·Risk Class 2·MD·OSTEOGENICS BIOMEDICAL, INC.·Registered Dec 29, 2017 – Dec 29, 2027ActiveRegistration details
- Analysis ID
- 03e52e70f3bfa7efef60fe23e6b43f05
- License Form
- Ministry of Health Medical Device Import No. 030668
- Customs Code
- DHA05603066803
Company information
- Manufacturer
- OSTEOGENICS BIOMEDICAL, INC.
- Manufacturer Country
- United States
- Authorized Representative
- OSSTEM CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I5035 Non-absorbent expanded PTFE surgical sutures
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 29, 2017
- Expiry Date
- Dec 29, 2027
About this record
Access comprehensive regulatory information for “Cytoplast” PTFE Suture in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 03e52e70f3bfa7efef60fe23e6b43f05 and manufactured by OSTEOGENICS BIOMEDICAL, INC.. The authorized representative in Taiwan is OSSTEM CORPORATION.
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