Taiwan FDA registration 05cb10e2b19520bb66805d5969fe2984

Synctoplasma pneumonia antibody reagent (unsterilized)

TW: 協克黴漿菌肺炎抗體試劑 (未滅菌)

Taiwan·Risk Class 1·EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG·Registered Oct 19, 2010 – Oct 19, 2025Expired

Registration details

Analysis ID: 05cb10e2b19520bb66805d5969fe2984
Customs Code: DHA04400938506

Company information

Manufacturer: EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG
Manufacturer Country: Germany
Authorized Representative: SEEKERS BIOMEDICAL CO., LTD.

Product details

Intended Use: Limited to the classification and grading management method of medical equipment, the first level identification range of "Mycoplasma serum reagent (C.3375)".
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3375 黴漿菌屬血清試劑
Import Information: import

Dates and status

Registration Date: Oct 19, 2010
Expiry Date: Oct 19, 2025

About this record

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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