Taiwan FDA registration d21a81200b63578a34fd90b07b859230

"Intermedic" Difficult Clostridium Toxin A+B Rapid Test Reagent (Unsterilized)　

TW: "英特邁迪克" 困難腸梭菌毒素A+B快速檢測試劑 (未滅菌)　

Taiwan·Risk Class 1·INTERMEDICAL·Registered Jan 30, 2013 – Jan 30, 2023Expired

Registration details

Analysis ID: d21a81200b63578a34fd90b07b859230
Customs Code: DHA04401265506

Company information

Manufacturer: INTERMEDICAL
Manufacturer Country: Italy
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: Jan 30, 2013
Expiry Date: Jan 30, 2023

About this record

Access comprehensive regulatory information for "Intermedic" Difficult Clostridium Toxin A+B Rapid Test Reagent (Unsterilized)　 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d21a81200b63578a34fd90b07b859230 and manufactured by INTERMEDICAL. The authorized representative in Taiwan is GHOPE INTERNATIONAL BIOTECHNOLOGY CO., LTD..

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