Taiwan FDA registration 4509d215b41dfcd04aaebc2001a23413
Kenda Abrasive Series (Unsterilized)
TW: 肯達研磨材系列 (未滅菌)
Taiwan·Risk Class 1·KENDA AG·Registered Apr 07, 2006 – Apr 07, 2011CancelledRegistration details
- Analysis ID
- 4509d215b41dfcd04aaebc2001a23413
- Customs Code
- DHA04400349802
Company information
- Manufacturer
- KENDA AG
- Manufacturer Country
- Liechtenstein
- Authorized Representative
- Sanye Limited
Product details
- Intended Use
- It is limited to the first level of identification of the Administrative Measures for Medical Devices (Grinding Devices and Their Annexes [F.6010]).
- Product Type (Level 1)
- F Dentistry
- Import Information
- import
Dates and status
- Registration Date
- Apr 07, 2006
- Expiry Date
- Apr 07, 2011
- Cancellation Date
- Jan 17, 2013
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Kenda Abrasive 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 4509d215b41dfcd04aaebc2001a23413 and manufactured by KENDA AG. The authorized representative in Taiwan is Sanye Limited.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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