Taiwan FDA registration e1b6c329ad28a7d05dab7622e1c57b4a
"Semei" Tieca's anterior cervical lamina system
TW: "西美" 提尼卡前方頸椎板系統
Taiwan·Risk Class 2·ZIMMER BIOMET SPINE, INC.·Registered Sep 14, 2005 – Sep 14, 2025ExpiredRegistration details
- Analysis ID
- e1b6c329ad28a7d05dab7622e1c57b4a
- Customs Code
- DHA00601190800
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 Orthopedics
- Product Type (Level 2)
- N.3060 椎體間之脊椎矯正固定物
- Import Information
- import
Dates and status
- Registration Date
- Sep 14, 2005
- Expiry Date
- Sep 14, 2025
About this record
Access comprehensive regulatory information for "Semei" Tieca's anterior cervical lamina system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e1b6c329ad28a7d05dab7622e1c57b4a and manufactured by ZIMMER BIOMET SPINE, INC.. The authorized representative in Taiwan is ZimVie Taiwan Co., Ltd..
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