Taiwan FDA registration 0120ac6438cf26c0ee7e1fa66b3cf83c
Jedon Denture Adhesive Paste (Unsterilized)
TW: 潔登保潔靈假牙黏著膏(未滅菌)
Taiwan·Risk Class 1·QUEISSER PHARMA GMBH & CO., KG·Registered Oct 28, 2005 – Oct 28, 2015CancelledRegistration details
- Analysis ID
- 0120ac6438cf26c0ee7e1fa66b3cf83c
- Customs Code
- DHA04400134608
Company information
- Manufacturer
- QUEISSER PHARMA GMBH & CO., KG
- Manufacturer Country
- Germany
- Authorized Representative
- BEST OCEAN PHARMACEUTICAL CO., LTD.
Product details
- Intended Use
- Dentures are applied to the base of the denture before being placed in the patient's mouth to increase the retention and comfort of the denture.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3490 Aminomethyl fiber-vigan metal, and/or polyethylene methyl ether butylate calcium butylate calcium compound denture adhesive
- Import Information
- import
Dates and status
- Registration Date
- Oct 28, 2005
- Expiry Date
- Oct 28, 2015
- Cancellation Date
- Aug 14, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Jedon Denture Adhesive Paste (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0120ac6438cf26c0ee7e1fa66b3cf83c and manufactured by QUEISSER PHARMA GMBH & CO., KG. The authorized representative in Taiwan is BEST OCEAN PHARMACEUTICAL CO., LTD..
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