Taiwan FDA registration f7e0ead3a0a9e4be7cd3791ab745f8a5
"Keshira" Brak dental implant machine and its accessories (unsterilized)
TW: "克希拉" 布拉克植牙機及其附件(未滅菌)
Taiwan·Risk Class 1·KYOCERA MEDICAL CORPORATION·Registered Mar 20, 2012 – Mar 20, 2017CancelledRegistration details
- Analysis ID
- f7e0ead3a0a9e4be7cd3791ab745f8a5
- Customs Code
- DHA04401150508
Company information
- Manufacturer
- KYOCERA MEDICAL CORPORATION
- Manufacturer Country
- Japan
- Authorized Representative
- AYERS MEDICAL TRADING CORP.
Product details
- Intended Use
- Limited to the first level recognition range of medical equipment management measures dental handpieces and their accessories (F.4200).
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.4200 Dental handset and accessories thereof
- Import Information
- import
Dates and status
- Registration Date
- Mar 20, 2012
- Expiry Date
- Mar 20, 2017
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Keshira" Brak dental implant machine and its accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f7e0ead3a0a9e4be7cd3791ab745f8a5 and manufactured by KYOCERA MEDICAL CORPORATION. The authorized representative in Taiwan is AYERS MEDICAL TRADING CORP..
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.
Free DatabasePowered by Pure Global AI89,000+ Devices