Taiwan FDA registration e71e1d25fdde8b0cc654ecd84ab50948
"VEDA" C.D. (C. Difficile) GDH-Check-1(Non-Sterile)
TW: "委達" 梭羅桿菌毒素A+B快速測試片(未滅菌)
Taiwan·Risk Class 1·MD·VEDA LAB·Registered Jun 10, 2014 – Jun 10, 2019CancelledRegistration details
- Analysis ID
- e71e1d25fdde8b0cc654ecd84ab50948
- License Form
- Ministry of Health Medical Device Import No. 014229
- Customs Code
- DHA09401422905
Company information
- Manufacturer
- VEDA LAB
- Manufacturer Country
- France
- Authorized Representative
- RAFA INTERNATIONAL CORP.
Product details
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C2660 Microbial identification and assay equipment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 10, 2014
- Expiry Date
- Jun 10, 2019
- Cancellation Date
- Apr 08, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "VEDA" C.D. (C. Difficile) GDH-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 e71e1d25fdde8b0cc654ecd84ab50948 and manufactured by VEDA LAB. The authorized representative in Taiwan is RAFA INTERNATIONAL CORP..
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