Taiwan FDA registration 64492a2cce6ca5e0241823d12678c6e5
"Shin Sheng" Lancing device (Non-Sterile)
TW: "幸生" 採血筆 (未滅菌)
Taiwan·Risk Class 1·MD·GMMC·Registered Jan 27, 2014 – Jan 27, 2019CancelledRegistration details
- Analysis ID
- 64492a2cce6ca5e0241823d12678c6e5
- License Form
- Ministry of Health Medical Device Import No. 013811
- Customs Code
- DHA09401381105
Company information
- Manufacturer
- GMMC
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- SHIN SHENG PHARMACEUTICAL CO., LTD.
Product details
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
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 "Shin Sheng" Lancing device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 64492a2cce6ca5e0241823d12678c6e5 and manufactured by GMMC. The authorized representative in Taiwan is SHIN SHENG PHARMACEUTICAL CO., LTD..
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