Taiwan FDA registration 9e2299fb9e07290dae8208eae9811c0b

“Bio-Rad” Disks for Antibiotic Susceptibilty Testing-Drug Group of Urinary Tract Infection

TW: “伯瑞” 抗生素感受性試驗紙錠-抗泌尿道感染劑類
Taiwan flagTaiwan·Risk Class 2·MD·BIO-RAD·Registered Sep 15, 2015 – Sep 15, 2025Expired
Registration details
Analysis ID
9e2299fb9e07290dae8208eae9811c0b
License Form
Ministry of Health Medical Device Import No. 027675
Customs Code
DHA05602767503
Company information
Manufacturer
BIO-RAD
Manufacturer Country
France
Product details
Intended Use
These ingot are used to semi-quantitatively assess the in vitro drug susceptibility of fast-growing bacteria and several uncontrollable strains against urinary tract infectious agents and antimicrobials by agar diffusion.
Product Type (Level 1)
C Immunology and microbiology devices
Product Type (Level 2)
C1620 Antimicrobial susceptibility test tray
Import Information
Imported from abroad
Dates and status
Registration Date
Sep 15, 2015
Expiry Date
Sep 15, 2025
About this record

Access comprehensive regulatory information for “Bio-Rad” Disks for Antibiotic Susceptibilty Testing-Drug Group of Urinary Tract Infection in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9e2299fb9e07290dae8208eae9811c0b and manufactured by BIO-RAD. The authorized representative in Taiwan is Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.).

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