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)
Taiwan flagTaiwan·Risk Class 1·VEDA. LAB·Registered Apr 03, 2012 – Apr 03, 2017Cancelled
Registration details
Analysis ID
d67ef74a891e56323c8823ea78f12bfa
Customs Code
DHA04401156207
Company information
Manufacturer
VEDA. LAB
Manufacturer Country
France
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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