Taiwan FDA registration 409660fa485b28aa15b8e1efcacbfd90

"ImmuneMed" Leptospira (Non-Sterile)

TW: "醫誠" 鉤端螺旋體抗體快速檢驗試劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·IMMUNEMED, INC.·Registered Jun 20, 2019 – Jun 20, 2024Expired
Registration details
Analysis ID
409660fa485b28aa15b8e1efcacbfd90
License Form
Ministry of Health Medical Device Import No. 020573
Customs Code
DHA09402057306
Company information
Manufacturer
IMMUNEMED, INC.
Manufacturer Country
Korea, Republic of
Authorized Representative
EUGENE-CHEN CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the medical device management measures "Leptospira sera reagent (C.3350)".
Product Type (Level 1)
C Immunology and microbiology devices
Product Type (Level 2)
C3350 Leptospira serology
Import Information
Imported from abroad
Dates and status
Registration Date
Jun 20, 2019
Expiry Date
Jun 20, 2024
About this record

Access comprehensive regulatory information for "ImmuneMed" Leptospira (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 409660fa485b28aa15b8e1efcacbfd90 and manufactured by IMMUNEMED, INC.. 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.

Free DatabasePowered by Pure Global AI89,000+ Devices