Taiwan FDA registration 04752a4cc12bc4be5afca01bbfaa89dc
"Kunibi" General Surgical Instrument (Unsterilized)
TW: "邦美" 一般手術器械 (未滅菌)
Taiwan·Risk Class 1·BIOMET ORTHOPEDICS·Registered Jan 26, 2011 – Jan 26, 2021CancelledRegistration details
- Analysis ID
- 04752a4cc12bc4be5afca01bbfaa89dc
- Customs Code
- DHA04400985902
Company information
- Manufacturer
- BIOMET ORTHOPEDICS
- Manufacturer Country
- United States
- Authorized Representative
- MEDLION BIOTECH CO., LTD.
Product details
- Intended Use
- vacuum
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- import
Dates and status
- Registration Date
- Jan 26, 2011
- Expiry Date
- Jan 26, 2021
- Cancellation Date
- Jul 19, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kunibi" General Surgical Instrument (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 04752a4cc12bc4be5afca01bbfaa89dc and manufactured by BIOMET ORTHOPEDICS. The authorized representative in Taiwan is MEDLION BIOTECH CO., LTD..
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