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"Vircell" Chlamydophila pneumoniae Test (Non-sterile) - Taiwan Registration 57dc29c46d2947d84bda44f2efbf506b

Access comprehensive regulatory information for "Vircell" Chlamydophila pneumoniae Test (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 57dc29c46d2947d84bda44f2efbf506b and manufactured by VIRCELL, S.L. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..

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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57dc29c46d2947d84bda44f2efbf506b
Registration Details
Taiwan FDA Registration: 57dc29c46d2947d84bda44f2efbf506b
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Device Details

"Vircell" Chlamydophila pneumoniae Test (Non-sterile)
TW: "ๅ‡ก่ณฝ็ˆพ" ่‚บ็‚ŽๆŠซ่กฃ่Œๆชขๆธฌ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

57dc29c46d2947d84bda44f2efbf506b

Ministry of Health Medical Device Import No. 017331

DHA09401733101

Company Information

Spain

Product Details

Limited to the first level identification range of Chlamydomydia serum reagent (C.3120) of medical device management methods.

C Immunology and microbiology devices

C3120 Chlamydia serum reagent

Imported from abroad

Dates and Status

Dec 22, 2016

Dec 22, 2026