Taiwan FDA registration e6fd006493107c706b6d32e6a945f20a
"Fuyong" Leisho disposable blood lancet (sterilization)
TW: "福永" 雷碩拋棄式採血針 (滅菌)
Taiwan·Risk Class 1·GMMC·Registered Apr 24, 2012 – Apr 24, 2017CancelledRegistration details
- Analysis ID
- e6fd006493107c706b6d32e6a945f20a
- Customs Code
- DHA04401162008
Company information
- Manufacturer
- GMMC
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- EPS BIO TECHNOLOGY CORP.
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
- Apr 24, 2012
- Expiry Date
- Apr 24, 2017
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Fuyong" Leisho disposable blood lancet (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e6fd006493107c706b6d32e6a945f20a and manufactured by GMMC. The authorized representative in Taiwan is EPS BIO TECHNOLOGY CORP..
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