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"R-Biopharm" RIDAGENE Mycoplasma pneumoniae kit (Non-sterile) - Taiwan Registration ecd8d4daa7975f966514abdf3665eb12

Access comprehensive regulatory information for "R-Biopharm" RIDAGENE Mycoplasma pneumoniae kit (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 ecd8d4daa7975f966514abdf3665eb12 and manufactured by R-BIOPHARM AG. The authorized representative in Taiwan is METEK LAB INC..

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ecd8d4daa7975f966514abdf3665eb12
Registration Details
Taiwan FDA Registration: ecd8d4daa7975f966514abdf3665eb12
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Device Details

"R-Biopharm" RIDAGENE Mycoplasma pneumoniae kit (Non-sterile)
TW: "ๅšๆ–น" ่‚บ็‚Ž้ปดๆผฟ่Œๆชขๆธฌ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

ecd8d4daa7975f966514abdf3665eb12

Ministry of Health Medical Device Import No. 015712

DHA09401571200

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

Oct 02, 2015

Oct 02, 2025