Taiwan FDA registration e0563f20812dd80e4f8b486c15e5202d
"VEDA" S. PNEUMO-CHECK-1 (Non-Sterile)
TW: "委達" 肺炎鏈球菌尿液抗原檢測試劑 (未滅菌)
Taiwan·Risk Class 1·MD·VEDA LAB·Registered May 04, 2016 – May 04, 2026ExpiredRegistration details
- Analysis ID
- e0563f20812dd80e4f8b486c15e5202d
- License Form
- Ministry of Health Medical Device Import No. 016488
- Customs Code
- DHA09401648800
Company information
- Manufacturer
- VEDA LAB
- Manufacturer Country
- France
- Authorized Representative
- RAFA INTERNATIONAL CORP.
Product details
- Intended Use
- Restriction of medical device management methods Streptococcus belongs to the first level identification range of serum reagent (C.3740).
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3740 Streptococcus serology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 04, 2016
- Expiry Date
- May 04, 2026
About this record
Access comprehensive regulatory information for "VEDA" S. PNEUMO-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 e0563f20812dd80e4f8b486c15e5202d 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