Taiwan FDA registration 22619e2ce7a034e3ad230054f3e56407
"Commissioner" rotavirus/adenovirus 2-in-1 rapid test reagent (unsterilized)
TW: “委達”輪狀病毒/腺病毒 二合一快速檢驗試劑(未滅菌)
Taiwan·Risk Class 1·VEDA LAB·Registered Jun 16, 2014 – Jun 16, 2019CancelledRegistration details
- Analysis ID
- 22619e2ce7a034e3ad230054f3e56407
- Customs Code
- DHA09401424809
Company information
- Manufacturer
- VEDA LAB
- Manufacturer Country
- France
- Authorized Representative
- RAFA INTERNATIONAL CORP.
Product details
- Intended Use
- Limited to the first level of identification range of "polio virus serum reagent (C.3405)" and "adenovirus serum reagent (C.3020)" under the management measures for medical devices.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3020 腺病毒血清試劑;; C.3405 小兒麻痺病毒血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Jun 16, 2014
- Expiry Date
- Jun 16, 2019
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Commissioner" rotavirus/adenovirus 2-in-1 rapid test reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 22619e2ce7a034e3ad230054f3e56407 and manufactured by VEDA LAB. The authorized representative in Taiwan is RAFA INTERNATIONAL CORP..
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