Taiwan FDA registration 51b9707d4c2bae3086ddf67b08c317ab
"Certeri" must be adapted to Solo ultrasound dental instruments
TW: “賽特力”必適通索羅超音波牙科儀器
Taiwan·Risk Class 2·SATELEC, A COMPANY OF ACTEON GROUP·Registered Jul 04, 2013 – Jul 04, 2018CancelledRegistration details
- Analysis ID
- 51b9707d4c2bae3086ddf67b08c317ab
- Customs Code
- DHA00602515003
Company information
- Manufacturer
- SATELEC, A COMPANY OF ACTEON GROUP
- Manufacturer Country
- France
- Authorized Representative
- C&N MED-DENT CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.4120 Bone cutters and accessories thereof
- Import Information
- import
Dates and status
- Registration Date
- Jul 04, 2013
- Expiry Date
- Jul 04, 2018
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Certeri" must be adapted to Solo ultrasound dental instruments in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 51b9707d4c2bae3086ddf67b08c317ab and manufactured by SATELEC, A COMPANY OF ACTEON GROUP. The authorized representative in Taiwan is C&N MED-DENT CO., LTD..
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