Taiwan FDA registration a26e5812278b752de8c2419e5a79cc98
"VEDA" LEGIO-CHECK-1 (Non-Sterile)
TW: "委達" 退伍軍人肺炎尿液抗原檢測試劑 (未滅菌)
Taiwan·Risk Class 1·MD·VEDA LAB·Registered May 03, 2016 – May 03, 2021ExpiredRegistration details
- Analysis ID
- a26e5812278b752de8c2419e5a79cc98
- License Form
- Ministry of Health Medical Device Import No. 016482
- Customs Code
- DHA09401648201
Company information
- Manufacturer
- VEDA LAB
- Manufacturer Country
- France
- Authorized Representative
- RAFA INTERNATIONAL CORP.
Product details
- Intended Use
- Limit the management method of medical equipment Haemophilus serogenus (C.3300) first level identification range.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3300 Haemophilus serology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 03, 2016
- Expiry Date
- May 03, 2021
About this record
Access comprehensive regulatory information for "VEDA" LEGIO-CHECK-1 (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 a26e5812278b752de8c2419e5a79cc98 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