Taiwan FDA registration c1b4f39847d80900fb96cdcc93e3fab6

"Thermo Fisher Scientific" Mycoplasma spp. serological reagents (Non-Sterile)

TW: "賽默飛世爾科技" 黴漿菌屬血清試劑 (未滅菌)

Taiwan·Risk Class 1·MD·REMEL INC.·Registered Oct 13, 2016 – Oct 13, 2021Expired

Registration details

Analysis ID: c1b4f39847d80900fb96cdcc93e3fab6
License Form: Ministry of Health Medical Device Import No. 017078
Customs Code: DHA09401707802

Company information

Manufacturer: REMEL INC.
Manufacturer Country: United States
Authorized Representative: THERMO FISHER SCIENTIFIC TAIWAN CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Mycoplasma Serological Reagent (C.3375)".
Product Type (Level 1): C Immunology and microbiology devices
Product Type (Level 2): C3375 Mycoplasma serum reagent
Import Information: Imported from abroad

Dates and status

Registration Date: Oct 13, 2016
Expiry Date: Oct 13, 2021

About this record

Access comprehensive regulatory information for "Thermo Fisher Scientific" Mycoplasma spp. 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 c1b4f39847d80900fb96cdcc93e3fab6 and manufactured by REMEL INC.. The authorized representative in Taiwan is THERMO FISHER SCIENTIFIC TAIWAN CO., LTD..

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