Pure Global
Taiwan FDA registration 0577302791e1d7c13e37dc8ea2b4c475

Respiratory Fusion Virus Rapid Test (Unsterilized)

TW: 委達呼吸道融合病毒快速檢測片(未滅菌)
Taiwan flagTaiwan·Risk Class 1·VEDA LAB·Registered Oct 12, 2005 – Oct 12, 2025Expired
Registration details
Analysis ID
0577302791e1d7c13e37dc8ea2b4c475
Customs Code
DHA04400089408
Company information
Manufacturer
VEDA LAB
Manufacturer Country
France
Authorized Representative
RAFA INTERNATIONAL CORP.
Product details
Intended Use
Detection of respiratory cell fusion virus (RSV) using the principle of immunochromatography.
Product Type (Level 1)
C Immunology and microbiology
Product Type (Level 2)
C.3480 呼吸道融合細胞病毒血清試劑
Import Information
import
Dates and status
Registration Date
Oct 12, 2005
Expiry Date
Oct 12, 2025
About this record

Access comprehensive regulatory information for Respiratory Fusion Virus Rapid Test (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0577302791e1d7c13e37dc8ea2b4c475 and manufactured by VEDA LAB. The authorized representative in Taiwan is RAFA INTERNATIONAL CORP..

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