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"R-Biopharm" Mycoplasma Pneumoniae Test (non-sterile) - Taiwan Registration 59dd02e646a9523b90a68786ce40aca3

Access comprehensive regulatory information for "R-Biopharm" Mycoplasma 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 59dd02e646a9523b90a68786ce40aca3 and manufactured by R-BIOPHARM AG. The authorized representative in Taiwan is TRUGENE DIAGNOSTICS, INC..

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59dd02e646a9523b90a68786ce40aca3
Registration Details
Taiwan FDA Registration: 59dd02e646a9523b90a68786ce40aca3
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Device Details

"R-Biopharm" Mycoplasma Pneumoniae Test (non-sterile)
TW: "ๅ…ซๆ–น" ่‚บ็‚Ž้ปดๆผฟ่Œๆชขๆธฌ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

59dd02e646a9523b90a68786ce40aca3

Ministry of Health Medical Device Import No. 013865

DHA09401386502

Company Information

Germany

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Mycoplasma Serological Reagent (C.3375)".

C Immunology and microbiology devices

C3375 Mycoplasma serum reagent

Imported from abroad

Dates and Status

Feb 21, 2014

Feb 21, 2024