Taiwan FDA registration cc13efffdd873dca9a787614a63b65a5
"Aois" denture liner (unsterilized)
TW: “葵斯”假牙襯墊 (未滅菌)
Taiwan·Risk Class 1·QUEISSER PHARMA GMBH & CO., KG·Registered Jun 30, 2008 – Jun 30, 2018CancelledRegistration details
- Analysis ID
- cc13efffdd873dca9a787614a63b65a5
- Customs Code
- DHA04400684805
Company information
- Manufacturer
- QUEISSER PHARMA GMBH & CO., KG
- Manufacturer Country
- Germany
- Authorized Representative
- BEST OCEAN PHARMACEUTICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of denture liners (F.3540) of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3540 No prescription denture pad required
- Import Information
- import
Dates and status
- Registration Date
- Jun 30, 2008
- Expiry Date
- Jun 30, 2018
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Aois" denture liner (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cc13efffdd873dca9a787614a63b65a5 and manufactured by QUEISSER PHARMA GMBH & CO., KG. The authorized representative in Taiwan is BEST OCEAN PHARMACEUTICAL CO., LTD..
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