Taiwan FDA registration fc4aebd9f774ffbf55ded5f67561955b
"Kumabi" manual instrument for general surgery (unsterilized)
TW: “熊牌” 一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·BEAR MEDIC CORPORATION·Registered Sep 15, 2009 – Sep 15, 2019CancelledRegistration details
- Analysis ID
- fc4aebd9f774ffbf55ded5f67561955b
- Customs Code
- DHA04400810001
Company information
- Manufacturer
- BEAR MEDIC CORPORATION
- Manufacturer Country
- Japan
- Authorized Representative
- MIN SHIN INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- 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
- Sep 15, 2009
- Expiry Date
- Sep 15, 2019
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kumabi" manual instrument for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fc4aebd9f774ffbf55ded5f67561955b and manufactured by BEAR MEDIC CORPORATION. The authorized representative in Taiwan is MIN SHIN INSTRUMENTS CO., LTD..
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