Taiwan FDA registration 6f39e01596a603f43a02302238c71598

"DIASORIN INC" Adenovirus serological reagents (Non-Sterile)

TW: "禮亞尚" 腺病毒血清試劑 (未滅菌)

Taiwan·Risk Class 1·MD·DIASORIN INC.·Registered Sep 10, 2020 – Sep 10, 2025Expired

Registration details

Analysis ID: 6f39e01596a603f43a02302238c71598
License Form: Ministry of Health Medical Device Import No. 021957
Customs Code: DHA09402195703

Company information

Manufacturer: DIASORIN INC.
Manufacturer Country: United States
Authorized Representative: EVERLIGHT BIOTECH(TAIWAN) CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Adenovirus Serological Reagent (C.3020)".
Product Type (Level 1): C Immunology and microbiology devices
Product Type (Level 2): C3020 adenovirus serum reagent
Import Information: Imported from abroad

Dates and status

Registration Date: Sep 10, 2020
Expiry Date: Sep 10, 2025

About this record

Access comprehensive regulatory information for "DIASORIN INC" Adenovirus serological reagents (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 6f39e01596a603f43a02302238c71598 and manufactured by DIASORIN INC.. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..

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