Taiwan FDA registration e83f329fa223c0471143b1f5e022365d
"Jiemai" Surgical Device (Extinction/Incannificaculation)
TW: "捷邁" 手動式骨科手術器械(滅菌/未滅菌)
Taiwan·Risk Class 1·ZIMMER CAS·Registered Sep 21, 2023 – Sep 21, 2028ActiveRegistration details
- Analysis ID
- e83f329fa223c0471143b1f5e022365d
- Customs Code
- DHA09402325303
Company information
- Manufacturer
- ZIMMER CAS
- Manufacturer Country
- Canada
- Authorized Representative
- ZIMMER BIOMET TAIWAN CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management measures of medical equipment "Manual orthopedic surgical instruments (N.4540)" first grade identification range.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4540 手動式骨科手術器械
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Sep 21, 2023
- Expiry Date
- Sep 21, 2028
About this record
Access comprehensive regulatory information for "Jiemai" Surgical Device (Extinction/Incannificaculation) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e83f329fa223c0471143b1f5e022365d and manufactured by ZIMMER CAS. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..
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