Taiwan FDA registration f55b60ea68eb7783c5f1bebef97327ce
“Kulzer” Dental impression materials mixing device (Non-Sterile)
TW: “古莎”牙科印模材混合機(未滅菌)
Taiwan·Risk Class 1·MD·KULZER GMBH·Registered May 24, 2019 – May 24, 2024ExpiredRegistration details
- Analysis ID
- f55b60ea68eb7783c5f1bebef97327ce
- License Form
- Ministry of Health Medical Device Import No. 020485
- Customs Code
- DHA09402048509
Company information
- Manufacturer
- KULZER GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- ANDLIFE INC.
Product details
- Intended Use
- Limited to the first level identification range of dental and mercury instruments (F.3100) in the management of medical devices.
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3100 Dental and mercury ware
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 24, 2019
- Expiry Date
- May 24, 2024
About this record
Access comprehensive regulatory information for “Kulzer” Dental impression materials mixing device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f55b60ea68eb7783c5f1bebef97327ce and manufactured by KULZER GMBH. The authorized representative in Taiwan is ANDLIFE INC..
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