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"R-Biopharm" Legionella (Non-Sterile) - Taiwan Registration 5226783fc7189578a20fa43c01662021

Access comprehensive regulatory information for "R-Biopharm" 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 5226783fc7189578a20fa43c01662021 and manufactured by R-BIOPHARM AG. The authorized representative in Taiwan is METEK LAB INC..

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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5226783fc7189578a20fa43c01662021
Registration Details
Taiwan FDA Registration: 5226783fc7189578a20fa43c01662021
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Device Details

"R-Biopharm" Legionella (Non-Sterile)
TW: "ๅšๆ–น" ้€€ไผ่ปไบบ่‚บ็‚ŽๅฐฟๆถฒๆŠ—ๅŽŸๅฟซ้€Ÿ่จบๆ–ท่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

5226783fc7189578a20fa43c01662021

Ministry of Health Medical Device Import No. 018524

DHA09401852401

Company Information

Germany

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

Nov 20, 2017

Nov 20, 2022