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"CerTest" Legionella (Non-Sterile) - Taiwan Registration fbba6bdf466d05ddeeeb4dbcff751321

Access comprehensive regulatory information for "CerTest" Legionella (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 fbba6bdf466d05ddeeeb4dbcff751321 and manufactured by CERTEST BIOTEC S.L.. The authorized representative in Taiwan is MEDTRI 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.

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fbba6bdf466d05ddeeeb4dbcff751321
Registration Details
Taiwan FDA Registration: fbba6bdf466d05ddeeeb4dbcff751321
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Device Details

"CerTest" Legionella (Non-Sterile)
TW: "ๆ”็‰นๅธ" ้€€ไผ่ปไบบ่‚บ็‚ŽๅฐฟๆถฒๆŠ—ๅŽŸๅฟซ้€Ÿ่จบๆ–ท่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

fbba6bdf466d05ddeeeb4dbcff751321

Ministry of Health Medical Device Import No. 022068

DHA09402206803

Company Information

Spain

Product Details

Limit the management method of medical equipment Haemophilus serogenus (C.3300) first level identification range.

C Immunology and microbiology devices

C3300 Haemophilus serology

Imported from abroad

Dates and Status

Oct 29, 2020

Oct 29, 2025