Taiwan FDA registration 58e90882829b5b29385a38bb0e5ac44c
“Cayenne” Biowick X Implant
TW: “凱燕”百威艾克斯植入物
Taiwan·Risk Class 2·MD·Cayenne Medical, Inc.·Registered Dec 20, 2019 – Dec 20, 2024ExpiredRegistration details
- Analysis ID
- 58e90882829b5b29385a38bb0e5ac44c
- License Form
- Ministry of Health Medical Device Import No. 033028
- Customs Code
- DHA05603302808
Company information
- Manufacturer
- Cayenne Medical, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- ZIMMER BIOMET TAIWAN CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3040 Smooth or threaded metal bone fixation
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 20, 2019
- Expiry Date
- Dec 20, 2024
About this record
Access comprehensive regulatory information for “Cayenne” Biowick X Implant in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 58e90882829b5b29385a38bb0e5ac44c and manufactured by Cayenne Medical, Inc.. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..
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