Taiwan FDA registration 416ee5507d73f47994f0ae1dab5a4bf7
"De Tower" dental equipment (unsterilized)
TW: “得擂塔”牙科用器械 (未滅菌)
Taiwan·Risk Class 1·DIRECT AB·Registered Jul 16, 2008 – Jul 16, 2018CancelledRegistration details
- Analysis ID
- 416ee5507d73f47994f0ae1dab5a4bf7
- Customs Code
- DHA04400692803
Company information
- Manufacturer
- DIRECT AB
- Manufacturer Country
- Sweden
- Authorized Representative
- ADVANCE DEVELOPMENT INC.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Dental Hand Instruments (F.4565)".
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.4565 牙科手用器械
- Import Information
- import
Dates and status
- Registration Date
- Jul 16, 2008
- Expiry Date
- Jul 16, 2018
- Cancellation Date
- Jun 17, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期;;自行鍵入
About this record
Access comprehensive regulatory information for "De Tower" dental equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 416ee5507d73f47994f0ae1dab5a4bf7 and manufactured by DIRECT AB. The authorized representative in Taiwan is ADVANCE DEVELOPMENT INC..
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