Taiwan FDA registration 512739e56d7d79c0b8594367c307f805
Tenderfoot Heel Incision Device (Sterile)
TW: 疼得福腳跟採血器(滅菌)
Taiwan·Risk Class 1·MD·Accriva Diagnostics Inc.·Registered Dec 19, 2017 – Dec 19, 2027ActiveRegistration details
- Analysis ID
- 512739e56d7d79c0b8594367c307f805
- License Form
- Ministry of Health Medical Device Import No. 018624
- Customs Code
- DHA09401862405
Company information
- Manufacturer
- Accriva Diagnostics Inc.
- 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
- Dec 19, 2017
- Expiry Date
- Dec 19, 2027
About this record
Access comprehensive regulatory information for Tenderfoot Heel Incision Device (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 512739e56d7d79c0b8594367c307f805 and manufactured by Accriva Diagnostics Inc.. The authorized representative in Taiwan is BioChain Co., Ltd..
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