Taiwan FDA registration 1a8baaa1cfae2af612e11a95f2edfbc7

Omega Gate Antimicrobial H antigens A, B, C, D and O antigens A, B, C, D test (not extinguished)

TW: 奧米加沙門抗菌 H 抗原 a,b, c, d 及 O 抗原 A, B, C, D 試劑(未滅菌)

Taiwan·Risk Class 1·OMEGA DIAGNOSTICS LTD.·Registered Nov 11, 2005 – Nov 11, 2020Cancelled

Registration details

Analysis ID: 1a8baaa1cfae2af612e11a95f2edfbc7
Customs Code: DHA04400188400

Company information

Manufacturer: OMEGA DIAGNOSTICS LTD.
Manufacturer Country: United Kingdom
Authorized Representative: EUGENE-CHEN CO., LTD.

Product details

Intended Use: This product is only suitable for in vitro diagnostic use to assist in the detection of Salmonella antibodies by slide agglutination or in vitro agglutination.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3550 沙門氏菌屬血清試劑
Import Information: import

Dates and status

Registration Date: Nov 11, 2005
Expiry Date: Nov 11, 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 Omega Gate Antimicrobial H antigens A, B, C, D and O antigens A, B, C, D test (not extinguished) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1a8baaa1cfae2af612e11a95f2edfbc7 and manufactured by OMEGA DIAGNOSTICS LTD.. The authorized representative in Taiwan is EUGENE-CHEN CO., LTD..

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