Taiwan FDA registration 91a4b5b5085189eae8bed23fb31c7687
"Kenda" grinding series (unsterilized)
TW: "肯達" 研磨材系列 (未滅菌)
Taiwan·Risk Class 1·KENDA AG VADUZ·Registered May 11, 2011 – May 11, 2021CancelledRegistration details
- Analysis ID
- 91a4b5b5085189eae8bed23fb31c7687
- Customs Code
- DHA04401034303
Company information
- Manufacturer
- KENDA AG VADUZ
- Manufacturer Country
- Liechtenstein
- Authorized Representative
- Sanye Limited
Product details
- Intended Use
- Limited to the first level identification range of grinding devices and their accessories (F.6010) under the management measures for medical equipment.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.6010 Abrasive devices and accessories thereof
- Import Information
- import
Dates and status
- Registration Date
- May 11, 2011
- Expiry Date
- May 11, 2021
- Cancellation Date
- Jun 15, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kenda" grinding series (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 91a4b5b5085189eae8bed23fb31c7687 and manufactured by KENDA AG VADUZ. The authorized representative in Taiwan is Sanye Limited.
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