Taiwan FDA registration c601dfd66f8442a44247217427eab9cd
"Kobayashi" denture fixative (unsterilized)
TW: “小林”假牙固定劑（未滅菌）
Taiwan·Risk Class 1·KOBAYASHI PHARMACEUTICAL CO., LTD.·Registered Sep 19, 2007 – Sep 19, 2017CancelledRegistration details
- Analysis ID
- c601dfd66f8442a44247217427eab9cd
- Customs Code
- DHA04400615806
Company information
- Manufacturer
- KOBAYASHI PHARMACEUTICAL CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- Xile Enterprises Limited
Product details
- Intended Use
- Limited to the first level of identification range of medical equipment management measures "sodium amino methylcellulose, and/or polyethylene methyl ether calcium sodium maleic acid compound salt denture adhesive (F.3490)".
- 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
- Sep 19, 2007
- Expiry Date
- Sep 19, 2017
- Cancellation Date
- Nov 28, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kobayashi" denture fixative (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c601dfd66f8442a44247217427eab9cd and manufactured by KOBAYASHI PHARMACEUTICAL CO., LTD.. The authorized representative in Taiwan is Xile Enterprises Limited.
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