Taiwan FDA registration d67ef74a891e56323c8823ea78f12bfa
"Feeder" Difficult Clostridium Enterotoxin A+B Detection Reagent (Non-sterile)
TW: "飛達" 困難腸梭菌毒素A+B檢測試劑 (未滅菌)
Registration details
- Analysis ID
- d67ef74a891e56323c8823ea78f12bfa
- Customs Code
- DHA04401156207
Company information
- Manufacturer
- VEDA. LAB
- Manufacturer Country
- France
- Authorized Representative
- GHOPE INTERNATIONAL BIOTECHNOLOGY CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Identification and Measurement Equipment (C.2660)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.2660 微生物鑑別及測定器材
- Import Information
- import
Dates and status
- Registration Date
- Apr 03, 2012
- Expiry Date
- Apr 03, 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 "Feeder" Difficult Clostridium Enterotoxin A+B Detection Reagent (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 d67ef74a891e56323c8823ea78f12bfa and manufactured by VEDA. LAB. The authorized representative in Taiwan is GHOPE INTERNATIONAL BIOTECHNOLOGY CO., LTD..
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