Taiwan FDA registration ebcb95c9ee7dcb75be4af98e8beed011
"Editi" finger blood collection device (unsterilized)
TW: “艾帝西”手指採血器(未滅菌)
Taiwan·Risk Class 1·INTERNATIONAL TECHNIDYNE CORP.·Registered Jan 20, 2012 – Jan 20, 2017CancelledRegistration details
- Analysis ID
- ebcb95c9ee7dcb75be4af98e8beed011
- Customs Code
- DHA04401132009
Company information
- Manufacturer
- INTERNATIONAL TECHNIDYNE CORP.
- 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, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- import
Dates and status
- Registration Date
- Jan 20, 2012
- Expiry Date
- Jan 20, 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 "Editi" finger blood collection device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ebcb95c9ee7dcb75be4af98e8beed011 and manufactured by INTERNATIONAL TECHNIDYNE CORP.. The authorized representative in Taiwan is BioChain Co., Ltd..
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