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"Bioken" Krivour Adenovirus (Respiratory) Rapid Test Kit (Unsterilized)  - Taiwan Registration 850f1630c981b25eb73be3e8c751a1c2

Access comprehensive regulatory information for "Bioken" Krivour Adenovirus (Respiratory) Rapid Test Kit (Unsterilized)  in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 850f1630c981b25eb73be3e8c751a1c2 and manufactured by DENKA CO., LTD. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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850f1630c981b25eb73be3e8c751a1c2
Registration Details
Taiwan FDA Registration: 850f1630c981b25eb73be3e8c751a1c2
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Device Details

"Bioken" Krivour Adenovirus (Respiratory) Rapid Test Kit (Unsterilized) 
TW: "生研" 快納威 腺病毒(呼吸道)快速檢驗套組 (未滅菌) 
Risk Class 1

Registration Details

850f1630c981b25eb73be3e8c751a1c2

DHA04401189406

Company Information

Japan

Product Details

Limited to the first level identification range of the classification and grading management method of medical equipment "adenovirus serum reagent (C.3020)".

C Immunology and microbiology

C.3020 腺病毒血清試劑

import

Dates and Status

Jun 28, 2012

Jun 28, 2027