Taiwan FDA registration a42e5cc0979780e45e43143efa0175fb
"KaVo" endodontic pulp canal reamer (Non-sterile)
TW: "卡瓦" 根管髓腔擴齒鑽 (未滅菌)
Taiwan·Risk Class 1·MD·KALTENBACH & VOIGT GMBH·Registered Nov 05, 2014 – Nov 05, 2019CancelledRegistration details
- Analysis ID
- a42e5cc0979780e45e43143efa0175fb
- License Form
- Ministry of Health Medical Device Import No. 014627
- Customs Code
- DHA09401462704
Company information
- Manufacturer
- KALTENBACH & VOIGT GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- NOBEL BIOCARE TAIWAN CO., LTD.
Product details
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F4565 Hand instruments for dental use
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 05, 2014
- Expiry Date
- Nov 05, 2019
- 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 "KaVo" endodontic pulp canal reamer (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 a42e5cc0979780e45e43143efa0175fb and manufactured by KALTENBACH & VOIGT GMBH. The authorized representative in Taiwan is NOBEL BIOCARE TAIWAN CO., LTD..
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