Taiwan FDA registration 1e26f47172e457fb165819aeb54b3a70
"IBL" Mumps Virus Reagent (Non-Sterile)
TW: "艾博爾"腮腺炎病毒檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·MD·IBL INTERNATIONAL GMBH·Registered Dec 11, 2015 – Dec 11, 2020CancelledRegistration details
- Analysis ID
- 1e26f47172e457fb165819aeb54b3a70
- License Form
- Ministry of Health Medical Device Import No. 015965
- Customs Code
- DHA09401596503
Company information
- Manufacturer
- IBL INTERNATIONAL GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- WOLCH ENTERPRISES INC.
Product details
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3380 Mumps virus serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 11, 2015
- Expiry Date
- Dec 11, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "IBL" Mumps Virus Reagent (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 1e26f47172e457fb165819aeb54b3a70 and manufactured by IBL INTERNATIONAL GMBH. The authorized representative in Taiwan is WOLCH ENTERPRISES INC..
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