Pure Global

"bioMerieux" VITEK MS Mycobacterium/Nocardia Kit (Non-Sterile) - Taiwan Registration fe8d01e5975e62ef344b165ba086bf16

Access comprehensive regulatory information for "bioMerieux" VITEK MS Mycobacterium/Nocardia Kit (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 fe8d01e5975e62ef344b165ba086bf16 and manufactured by BIOMERIEUX SA. The authorized representative in Taiwan is Hong Kong Commercial Mรฉrieux 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 Database
Powered by Pure Global AI
89,000+ Devices
fe8d01e5975e62ef344b165ba086bf16
Registration Details
Taiwan FDA Registration: fe8d01e5975e62ef344b165ba086bf16
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"bioMerieux" VITEK MS Mycobacterium/Nocardia Kit (Non-Sterile)
TW: "็”Ÿ็‰ฉๆข…้‡ŒๅŸƒ" ๅˆ†ๆžๆกฟ่Œ/ๅฅดๅกๆฐ่Œๅ‰่™•็†่ฉฆๅŠ‘็ต„ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

fe8d01e5975e62ef344b165ba086bf16

Ministry of Health Medical Device Import No. 017610

DHA09401761002

Company Information

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Identification and Measurement Equipment (C.2660)".

C Immunology and microbiology devices

C2660 Microbial identification and assay equipment

Imported from abroad

Dates and Status

Mar 16, 2017

Mar 16, 2027