Taiwan FDA registration eb04f76c86ef23b1f10760edcc065b30

Legicobacterium Legionella antibody reagent (unsterilized)　

TW: 協克退伍軍人桿菌抗體試劑(未滅菌)　

Taiwan·Risk Class 1·EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG·Registered Sep 23, 2010 – Sep 23, 2025Expired

Registration details

Analysis ID: eb04f76c86ef23b1f10760edcc065b30
Customs Code: DHA04400923207

Company information

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

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: Sep 23, 2010
Expiry Date: Sep 23, 2025

About this record

Access comprehensive regulatory information for Legicobacterium Legionella 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 eb04f76c86ef23b1f10760edcc065b30 and manufactured by EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG. The authorized representative in Taiwan is SEEKERS BIOMEDICAL 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.