Taiwan FDA registration 5d45e7bba58c19efdcf619f3b5a92b8a
Commissioner Rotavirus Rapid Test Tablets (Unsterilized)
TW: 委達輪狀病毒快速檢測片(未滅菌)
Taiwan·Risk Class 1·VEDA LAB·Registered Oct 18, 2005 – Oct 18, 2025ExpiredRegistration details
- Analysis ID
- 5d45e7bba58c19efdcf619f3b5a92b8a
- Customs Code
- DHA04400100100
Company information
- Manufacturer
- VEDA LAB
- Manufacturer Country
- France
- Authorized Representative
- RAFA INTERNATIONAL CORP.
Product details
- Intended Use
- Screening stool samples.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3405 Poliomyelitis virus serum reagent
- Import Information
- import
Dates and status
- Registration Date
- Oct 18, 2005
- Expiry Date
- Oct 18, 2025
About this record
Access comprehensive regulatory information for Commissioner Rotavirus Rapid Test Tablets (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5d45e7bba58c19efdcf619f3b5a92b8a 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.
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