Taiwan FDA registration b295ad83b2806ad84ddd210ebcdb94f5
“Cayenne” Biowick Surelock Implant
TW: “凱燕”百威秀拉植入物
Taiwan·Risk Class 2·MD·Cayenne Medical, Inc.·Registered Oct 10, 2019 – Oct 10, 2024ExpiredRegistration details
- Analysis ID
- b295ad83b2806ad84ddd210ebcdb94f5
- License Form
- Ministry of Health Medical Device Import No. 032861
- Customs Code
- DHA05603286107
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
- Oct 10, 2019
- Expiry Date
- Oct 10, 2024
About this record
Access comprehensive regulatory information for “Cayenne” Biowick Surelock Implant in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b295ad83b2806ad84ddd210ebcdb94f5 and manufactured by Cayenne Medical, Inc.. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..
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