Taiwan FDA registration d5de22d733848682829d7a136b7359f7

"Mei Eliel" Baynex Staphylococcus aureus rapid diagnostic reagent (unsterilized)

TW: "美艾利爾"拜奈克思金黃色葡萄球菌快速診斷試劑(未滅菌)

Taiwan·Risk Class 1·ALERE SCARBOROUGH, INC.·Registered Apr 22, 2010 – Apr 22, 2020Cancelled

Registration details

Analysis ID: d5de22d733848682829d7a136b7359f7
Customs Code: DHA04400875801

Company information

Manufacturer: ALERE SCARBOROUGH, INC.
Manufacturer Country: United States
Authorized Representative: Ariel Health Inc

Product details

Intended Use: Limited to the first level identification range of the "Staphylococcus aureus serum reagent (C.3700)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3700 金黃色葡萄球菌血清試劑
Import Information: import

Dates and status

Registration Date: Apr 22, 2010
Expiry Date: Apr 22, 2020
Cancellation Date: Jul 15, 2022

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "Mei Eliel" Baynex Staphylococcus aureus rapid diagnostic 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 d5de22d733848682829d7a136b7359f7 and manufactured by ALERE SCARBOROUGH, INC.. The authorized representative in Taiwan is Ariel Health Inc.

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