Taiwan FDA registration 4bc7522e159385af173767681d1b6f98

“SD BIOSENSOR” STANDARD F Adeno Respi Ag FIA (Non-Sterile)

TW: “速得百森” 腺病毒(呼吸道)檢驗試劑(未滅菌)

Taiwan·Risk Class 1·MD·SD BIOSENSOR, Inc.·Registered Mar 11, 2021 – Mar 11, 2026Expired

Registration details

Analysis ID: 4bc7522e159385af173767681d1b6f98
License Form: Ministry of Health Medical Device Import No. 022380
Customs Code: DHA09402238005

Company information

Manufacturer: SD BIOSENSOR, Inc.
Manufacturer Country: Korea, Republic of
Authorized Representative: CREATIVE LIFE SCIENCE 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: Mar 11, 2021
Expiry Date: Mar 11, 2026

About this record

Access comprehensive regulatory information for “SD BIOSENSOR” STANDARD F Adeno Respi Ag FIA (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 4bc7522e159385af173767681d1b6f98 and manufactured by SD BIOSENSOR, Inc.. The authorized representative in Taiwan is CREATIVE LIFE SCIENCE CO., LTD..

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