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"IMMUNOCATCH" Legionella (Non-Sterile) - Taiwan Registration 7bd9955ce8dc6a7aa1eeb96f0cf85911

Access comprehensive regulatory information for "IMMUNOCATCH" 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 7bd9955ce8dc6a7aa1eeb96f0cf85911 and manufactured by EIKEN CHEMICAL CO., LTD.. 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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7bd9955ce8dc6a7aa1eeb96f0cf85911
Registration Details
Taiwan FDA Registration: 7bd9955ce8dc6a7aa1eeb96f0cf85911
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Device Details

"IMMUNOCATCH" Legionella (Non-Sterile)
TW: "่‰พ็พŽๅ‡ฑ็‰น" ้€€ไผ่ปไบบ่‚บ็‚ŽๅฐฟๆถฒๆŠ—ๅŽŸๅฟซ้€Ÿ่จบๆ–ท่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

7bd9955ce8dc6a7aa1eeb96f0cf85911

Ministry of Health Medical Device Import No. 020391

DHA09402039100

Company Information

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

May 02, 2019

May 02, 2024