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Synctoplasma pneumonia antibody reagent (unsterilized) - Taiwan Registration 05cb10e2b19520bb66805d5969fe2984

Access comprehensive regulatory information for Synctoplasma pneumonia antibody reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 05cb10e2b19520bb66805d5969fe2984 and manufactured by EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG. The authorized representative in Taiwan is SEEKERS BIOMEDICAL CO., LTD..

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05cb10e2b19520bb66805d5969fe2984
Registration Details
Taiwan FDA Registration: 05cb10e2b19520bb66805d5969fe2984
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Device Details

Synctoplasma pneumonia antibody reagent (unsterilized)
TW: ๅ”ๅ…‹้ปดๆผฟ่Œ่‚บ็‚ŽๆŠ—้ซ”่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

05cb10e2b19520bb66805d5969fe2984

DHA04400938506

Company Information

Product Details

Limited to the classification and grading management method of medical equipment, the first level identification range of "Mycoplasma serum reagent (C.3375)".

C Immunology and microbiology

C.3375 ้ปดๆผฟ่Œๅฑฌ่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Oct 19, 2010

Oct 19, 2025