Taiwan FDA registration cb50a6cbc34533f7fec29bd5e0d78129

Baynex Veteran Pneumonia Urine Antigen Test Card (Unsterilized)

TW: 拜奈克思退伍軍人肺炎尿液抗原檢驗卡(未滅菌)

Taiwan·Risk Class 1·Abbott Diagnostics Scarborough, Inc.·Registered Apr 27, 2012 – Apr 27, 2027Active

Registration details

Analysis ID: cb50a6cbc34533f7fec29bd5e0d78129
Customs Code: DHA04401163702

Company information

Manufacturer: Abbott Diagnostics Scarborough, Inc.
Manufacturer Country: United States
Authorized Representative: Abbott Rapid Diagnostics Health Corp.

Product details

Intended Use: It is limited to the first-level identification scope of Haemophilus serum reagent (C.3300) in the classification and grading management method of medical devices.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3300 嗜血桿菌屬血清試劑
Import Information: import

Dates and status

Registration Date: Apr 27, 2012
Expiry Date: Apr 27, 2027

About this record

Access comprehensive regulatory information for Baynex Veteran Pneumonia Urine Antigen Test Card (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cb50a6cbc34533f7fec29bd5e0d78129 and manufactured by Abbott Diagnostics Scarborough, Inc.. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..

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