Taiwan FDA registration 5f6e0b1c8d6151d6d6b819ddb69c54fc

"Thermo Fisher Scientific" Influenza virus serological reagents (Non-Sterile)

TW: "賽默飛世爾科技" 流行性感冒病毒血清試劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·REMEL INC.·Registered Dec 02, 2015 – Dec 02, 2020Cancelled
Registration details
Analysis ID
5f6e0b1c8d6151d6d6b819ddb69c54fc
License Form
Ministry of Health Medical Device Import No. 015920
Customs Code
DHA09401592007
Company information
Manufacturer
REMEL INC.
Manufacturer Country
United States
Product details
Product Type (Level 1)
C Immunology and microbiology devices
Product Type (Level 2)
C3330 Influenza virus serum reagent
Import Information
Imported from abroad
Dates and status
Registration Date
Dec 02, 2015
Expiry Date
Dec 02, 2020
Cancellation Date
Jun 16, 2022
Cancellation information
Status
Logged out
Reason
許可證已逾有效期未申請展延
About this record

Access comprehensive regulatory information for "Thermo Fisher Scientific" Influenza virus 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 5f6e0b1c8d6151d6d6b819ddb69c54fc 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.

Free DatabasePowered by Pure Global AI89,000+ Devices