Taiwan FDA registration 7e2861d800091c4c4cc7202016e17a9a
"Kava" dental diode laser device
TW: “卡瓦”牙科二極體雷射裝置
Taiwan·Risk Class 2·KALTENBACH & VOIGT GMBH·Registered Dec 30, 2008 – Dec 30, 2018CancelledRegistration details
- Analysis ID
- 7e2861d800091c4c4cc7202016e17a9a
- Customs Code
- DHA00601953906
Company information
- Manufacturer
- KALTENBACH & VOIGT GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- NOBEL BIOCARE TAIWAN CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4810 Lasers for general surgical, orthopaedic and dermatological use
- Import Information
- import
Dates and status
- Registration Date
- Dec 30, 2008
- Expiry Date
- Dec 30, 2018
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Kava" dental diode laser device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7e2861d800091c4c4cc7202016e17a9a and manufactured by KALTENBACH & VOIGT GMBH. The authorized representative in Taiwan is NOBEL BIOCARE TAIWAN CO., LTD..
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