Taiwan FDA registration 743646bbb03eb0075758036d2106c1e9

"bioMerieux" VITEK MS CHCA (Non-Sterile)

TW: "生物梅里埃" 微生物鑑別及測定器材 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·BIOMERIEUX SA·Registered Mar 01, 2017 – Mar 01, 2027Active
Registration details
Analysis ID
743646bbb03eb0075758036d2106c1e9
License Form
Ministry of Health Medical Device Import No. 017535
Customs Code
DHA09401753501
Company information
Manufacturer
BIOMERIEUX SA
Manufacturer Country
France
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Identification and Measurement Equipment (C.2660)".
Product Type (Level 1)
C Immunology and microbiology devices
Product Type (Level 2)
C2660 Microbial identification and assay equipment
Import Information
Imported from abroad
Dates and status
Registration Date
Mar 01, 2017
Expiry Date
Mar 01, 2027
About this record

Access comprehensive regulatory information for "bioMerieux" VITEK MS CHCA (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 743646bbb03eb0075758036d2106c1e9 and manufactured by BIOMERIEUX SA. The authorized representative in Taiwan is Hong Kong Commercial Mérieux S.p.A. Taiwan Branch.

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