Taiwan FDA registration 92607ab9b1366feb60238bb0bf8b575f
“Zimmer Biomet Spine” Zyston Spacer System
TW: “捷邁”捷適登椎間穩定系統
Taiwan·Risk Class 2·MD·ZIMMER BIOMET SPINE, INC.·Registered May 08, 2018 – May 08, 2028ActiveRegistration details
- Analysis ID
- 92607ab9b1366feb60238bb0bf8b575f
- License Form
- Ministry of Health Medical Device Import No. 031066
- Customs Code
- DHA05603106606
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 08, 2018
- Expiry Date
- May 08, 2028
About this record
Access comprehensive regulatory information for “Zimmer Biomet Spine” Zyston Spacer System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 92607ab9b1366feb60238bb0bf8b575f and manufactured by ZIMMER BIOMET SPINE, INC.. The authorized representative in Taiwan is ZimVie Taiwan Co., Ltd..
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