Taiwan FDA registration 609d7c29006c40f6ec556045845ae1aa
“Zimmer Biomet Spine” Timberline MPF System
TW: “捷邁”帝博萊脊椎融合系統
Taiwan·Risk Class 2·MD·ZIMMER BIOMET SPINE, INC.·Registered May 16, 2020 – May 16, 2025ExpiredRegistration details
- Analysis ID
- 609d7c29006c40f6ec556045845ae1aa
- License Form
- Ministry of Health Medical Device Import No. 033647
- Customs Code
- DHA05603364700
Company information
- Manufacturer
- ZIMMER BIOMET SPINE, INC.
- Manufacturer Country
- United States
- Authorized Representative
- ZimVie 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)
- N3080 Interbody fusion device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 16, 2020
- Expiry Date
- May 16, 2025
About this record
Access comprehensive regulatory information for “Zimmer Biomet Spine” Timberline MPF System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 609d7c29006c40f6ec556045845ae1aa and manufactured by ZIMMER BIOMET SPINE, INC.. The authorized representative in Taiwan is ZimVie Taiwan Co., Ltd..
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