Taiwan FDA registration 96341df1cd88e060d79260b562781096

Omega Proteus OX2, OX19, OXK antigen reagents

TW: 奧米加變形桿菌OX2, OX19, OXK抗原試劑

Taiwan·Risk Class 1·OMEGA DIAGNOSTICS LTD.·Registered Nov 09, 2005 – Nov 09, 2010Cancelled

Registration details

Analysis ID: 96341df1cd88e060d79260b562781096
Customs Code: DHA04400181402

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, using slide agglutination or test-tube agglutination to assist in the detection of Proteus antibodies.
Product Type (Level 1): C Immunology and microbiology
Import Information: import

Dates and status

Registration Date: Nov 09, 2005
Expiry Date: Nov 09, 2010
Cancellation Date: Oct 29, 2012

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Omega Proteus OX2, OX19, OXK antigen reagents in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 96341df1cd88e060d79260b562781096 and manufactured by OMEGA DIAGNOSTICS LTD.. The authorized representative in Taiwan is EUGENE-CHEN CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.