Taiwan FDA registration 4b1e0ae7bdbcef50c654123fd58f7323
"Medison Teckeni Estimate" Dental Implant Stabilization Analyzer (Unsterilized)
TW: “梅迪森泰科尼估登”牙科植體穩定分析儀 (未滅菌)
Taiwan·Risk Class 1·MEDIZINTECHNIK GULDEN E.K.·Registered Jul 10, 2013 – Jul 10, 2018CancelledRegistration details
- Analysis ID
- 4b1e0ae7bdbcef50c654123fd58f7323
- Customs Code
- DHA04401319503
Company information
- Manufacturer
- MEDIZINTECHNIK GULDEN E.K.
- Manufacturer Country
- Germany
- Authorized Representative
- DIO IMPLANT TAIWAN CORPORATION
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
- Jul 10, 2013
- Expiry Date
- Jul 10, 2018
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Medison Teckeni Estimate" Dental Implant Stabilization Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4b1e0ae7bdbcef50c654123fd58f7323 and manufactured by MEDIZINTECHNIK GULDEN E.K.. The authorized representative in Taiwan is DIO IMPLANT TAIWAN CORPORATION.
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