"Kunibi" Manual instrument for general surgery (sterile/unsterilized)
- Analysis ID
- ca7d364d183bddf36486192ed0b7f0cc
- Customs Code
- DHA09402256201
- Manufacturer
- BIOMET ORTHOPEDICS
- Manufacturer Country
- United States
- Authorized Representative
- ZIMMER BIOMET TAIWAN CO., LTD.
- Intended Use
- Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- Input;; QMS/QSD
- Registration Date
- Apr 29, 2021
- Expiry Date
- Apr 29, 2026
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Access comprehensive regulatory information for "Kunibi" Manual instrument for general surgery (sterile/unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ca7d364d183bddf36486192ed0b7f0cc and manufactured by BIOMET ORTHOPEDICS. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BIOMET SPORTS MEDICINE, and 1 recent registrations in the same category. 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.