Taiwan FDA registration 3fa1ead581d09c64a822ee8f54a3d87c

"ichroma" Anti-Streptolysin O (ASO) Reagent (Non-Sterile)

TW: "艾濶瑪"抗鏈球菌溶血素O試劑(未滅菌)

Taiwan·Risk Class 1·MD·Boditech Med Inc.·Registered Mar 30, 2021 – Mar 30, 2026Expired

Registration details

Analysis ID: 3fa1ead581d09c64a822ee8f54a3d87c
License Form: Ministry of Health Medical Device Import No. 022426
Customs Code: DHA09402242603

Company information

Manufacturer: Boditech Med Inc.
Manufacturer Country: Korea, Republic of
Authorized Representative: MEDRICH INSTRUMENT CO., LTD.

Product details

Intended Use: Limited to the management of medical devices: Streptococcus is an extracellular enzyme reagent (C.3720) in the first grade identification range.
Product Type (Level 1): C Immunology and microbiology devices
Product Type (Level 2): C3720 Streptococcus is an extracellular enzyme reagent
Import Information: Imported from abroad

Dates and status

Registration Date: Mar 30, 2021
Expiry Date: Mar 30, 2026

About this record

Access comprehensive regulatory information for "ichroma" Anti-Streptolysin O (ASO) 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 3fa1ead581d09c64a822ee8f54a3d87c and manufactured by Boditech Med Inc.. The authorized representative in Taiwan is MEDRICH INSTRUMENT CO., LTD..

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