Taiwan FDA registration 924a89d46cc8c78da9a7fb0da11b46d0

"Plasmatec" Proteus OX2, OX19, OXK antigen reagent (Non-Sterile)

TW: "醫誠"變形桿菌OX2, OX19, OXK 抗原試劑(未滅菌)

Taiwan·Risk Class 1·MD·LAB 21 HEALTHCARE LTD·Registered Feb 03, 2020 – Feb 03, 2025Expired

Registration details

Analysis ID: 924a89d46cc8c78da9a7fb0da11b46d0
License Form: Ministry of Health Medical Device Import No. 021222
Customs Code: DHA09402122208

Company information

Manufacturer: LAB 21 HEALTHCARE LTD
Manufacturer Country: United Kingdom
Authorized Representative: EUGENE-CHEN CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Weil-Felix Serological Reagent (C.3410)".
Product Type (Level 1): C Immunology and microbiology devices
Product Type (Level 2): C3410 Weil-Felix serum reagent
Import Information: Imported from abroad

Dates and status

Registration Date: Feb 03, 2020
Expiry Date: Feb 03, 2025

About this record

Access comprehensive regulatory information for "Plasmatec" Proteus OX2, OX19, OXK antigen reagent (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 924a89d46cc8c78da9a7fb0da11b46d0 and manufactured by LAB 21 HEALTHCARE 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.