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"Torch Combination" Veterans Urine Antigen Rapid Diagnostic Test for Pneumonia (Unwiped Bacteria) - Taiwan Registration 125ce88f75caa2d5df6f99886aa7f3ea

Access comprehensive regulatory information for "Torch Combination" Veterans Urine Antigen Rapid Diagnostic Test for Pneumonia (Unwiped Bacteria) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 125ce88f75caa2d5df6f99886aa7f3ea and manufactured by EIKEN CHEMICAL CO., LTD. NOGI PLANT.. The authorized representative in Taiwan is GHOPE INTERNATIONAL BIOTECHNOLOGY 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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125ce88f75caa2d5df6f99886aa7f3ea
Registration Details
Taiwan FDA Registration: 125ce88f75caa2d5df6f99886aa7f3ea
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Device Details

"Torch Combination" Veterans Urine Antigen Rapid Diagnostic Test for Pneumonia (Unwiped Bacteria)
TW: ใ€็‚ฌๅˆใ€ž้€€ไผ่ปไบบ่‚บ็‚ŽๅฐฟๆถฒๆŠ—ๅŽŸๅฟซ้€Ÿ่จบๆ–ท่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

125ce88f75caa2d5df6f99886aa7f3ea

DHA09402351102

Company Information

Product Details

It is limited to the first-level identification scope of Haemophilus serum reagent (C.3300) in the classification and grading management method of medical devices.

C Immunology and microbiology

C.3300 ๅ—œ่ก€ๆกฟ่Œๅฑฌ่ก€ๆธ…่ฉฆๅŠ‘

Input;; QMS/QSD

Dates and Status

Jun 17, 2024

Jun 17, 2029