Taiwan FDA registration a56f60ac1f160680326c89f39da536ce

“Thermo Fisher Scientific” Microbiological specimen collection and transport device (Non-Sterile)

TW: "賽默飛世爾科技" 微生物樣本收集及輸送器材 (未滅菌)

Taiwan·Risk Class 1·MD·REMEL INC.·Registered Jul 27, 2018 – Jul 27, 2023Expired

Registration details

Analysis ID: a56f60ac1f160680326c89f39da536ce
License Form: Ministry of Health Medical Device Import No. 019421
Customs Code: DHA09401942109

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 scope of the Measures for the Administration of Medical Devices "Microbial Sample Collection and Delivery Equipment (C.2900)".
Product Type (Level 1): C Immunology and microbiology devices
Product Type (Level 2): C2900 Microbial sample collection and delivery device
Import Information: Imported from abroad

Dates and status

Registration Date: Jul 27, 2018
Expiry Date: Jul 27, 2023

About this record

Access comprehensive regulatory information for “Thermo Fisher Scientific” Microbiological specimen collection and transport device (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 a56f60ac1f160680326c89f39da536ce and manufactured by REMEL INC.. The authorized representative in Taiwan is THERMO FISHER SCIENTIFIC TAIWAN CO., LTD..

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.