Taiwan FDA registration fef70dad3ad08ccb4abf9c024a339583
ApexBio Lancing Device (Non-sterile)
TW: 五鼎採血器(未滅菌)
Taiwan·Risk Class 1·MD·OWEN MUMFORD LIMITED·Registered Mar 16, 2018 – Mar 16, 2023ExpiredRegistration details
- Analysis ID
- fef70dad3ad08ccb4abf9c024a339583
- License Form
- Ministry of Health Medical Device Import No. 018902
- Customs Code
- DHA09401890207
Company information
- Manufacturer
- OWEN MUMFORD LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- APEX BIOTECHNOLOGY CORPORATION
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 and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 16, 2018
- Expiry Date
- Mar 16, 2023
About this record
Access comprehensive regulatory information for ApexBio 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 fef70dad3ad08ccb4abf9c024a339583 and manufactured by OWEN MUMFORD LIMITED. The authorized representative in Taiwan is APEX BIOTECHNOLOGY CORPORATION.
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