Taiwan FDA registration 081234ab8bc66bc2e8e6802a6b5ede93
"Kosei" blood collection needle (sterile)
TW: "幸生" 採血針 (滅菌)
Taiwan·Risk Class 1·GMMC·Registered Jan 27, 2014 – Jan 27, 2019CancelledRegistration details
- Analysis ID
- 081234ab8bc66bc2e8e6802a6b5ede93
- Customs Code
- DHA09401381207
Company information
- Manufacturer
- GMMC
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- SHIN SHENG PHARMACEUTICAL 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
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jan 27, 2014
- Expiry Date
- Jan 27, 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 "Kosei" blood collection needle (sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 081234ab8bc66bc2e8e6802a6b5ede93 and manufactured by GMMC. The authorized representative in Taiwan is SHIN SHENG PHARMACEUTICAL CO., LTD..
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