Taiwan FDA registration 44188efc26b23526f632fff436ff8ae0
"Accriva" Tenderlett Incision Instruments (Non-Sterile)
TW: "愛葵發" 手指採血器 (未滅菌)
Taiwan·Risk Class 1·MD·ACCRIVA DIAGNOSTICS·Registered Oct 27, 2016 – Oct 27, 2021ExpiredRegistration details
- Analysis ID
- 44188efc26b23526f632fff436ff8ae0
- License Form
- Ministry of Health Medical Device Import No. 017126
- Customs Code
- DHA09401712600
Company information
- Manufacturer
- ACCRIVA DIAGNOSTICS
- Manufacturer Country
- United States
- Authorized Representative
- BioChain 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 and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 27, 2016
- Expiry Date
- Oct 27, 2021
About this record
Access comprehensive regulatory information for "Accriva" Tenderlett Incision Instruments (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 44188efc26b23526f632fff436ff8ae0 and manufactured by ACCRIVA DIAGNOSTICS. The authorized representative in Taiwan is BioChain Co., Ltd..
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