Taiwan FDA registration 538db3416d1c44d55db7645818bdfd32
“KaVo” Titanium Blank
TW: “卡瓦”牙科鈦塊
Taiwan·Risk Class 2·MD·Kaltenbach & Voigt GmbH (KaVo)·Registered Nov 04, 2015 – Nov 04, 2020CancelledRegistration details
- Analysis ID
- 538db3416d1c44d55db7645818bdfd32
- License Form
- Ministry of Health Medical Device Import No. 027933
- Customs Code
- DHA05602793302
Company information
- Manufacturer
- Kaltenbach & Voigt GmbH (KaVo)
- Manufacturer Country
- Germany
- Authorized Representative
- Taiwan Kava Co., Ltd
Product details
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3710 Base metal alloy
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 04, 2015
- Expiry Date
- Nov 04, 2020
- Cancellation Date
- Mar 01, 2018
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for “KaVo” Titanium Blank in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 538db3416d1c44d55db7645818bdfd32 and manufactured by Kaltenbach & Voigt GmbH (KaVo). The authorized representative in Taiwan is Taiwan Kava 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