Taiwan FDA registration c7088f21a740a571d5e1dbe206c4bfc5
Polyflor Denture Whitening Tablets (Unsterilized)
TW: 保麗淨假牙淨白清潔錠 (未滅菌)
Taiwan·Risk Class 1·Block Drug Company, Inc.(A GlaxoSmithKline Company)·Registered Dec 18, 2012 – Dec 18, 2022CancelledRegistration details
- Analysis ID
- c7088f21a740a571d5e1dbe206c4bfc5
- Customs Code
- DHA04401250207
Company information
- Manufacturer Country
- United States
- Authorized Representative
- HALEON UK SERVICES LIMITED TAIWAN BRANCH
Product details
- Intended Use
- Limit to the first level of identification range of denture cleaner (F.3520) without prescription under the management measures of medical devices.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3520 Dental device cleaner not requiring prescription
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Dec 18, 2012
- Expiry Date
- Dec 18, 2022
- 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 Polyflor Denture Whitening Tablets (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c7088f21a740a571d5e1dbe206c4bfc5 and manufactured by Block Drug Company, Inc.(A GlaxoSmithKline Company). The authorized representative in Taiwan is HALEON UK SERVICES LIMITED TAIWAN BRANCH.
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