Taiwan FDA registration c4300775c3c44bd81722013dd977b484
"Respler" intraoral camera (unsterilized)
TW: "攝普樂"口內攝影機(未滅菌)
Taiwan·Risk Class 1·PUFF·Registered Jul 02, 2013 – Jul 02, 2018CancelledRegistration details
- Analysis ID
- c4300775c3c44bd81722013dd977b484
- Customs Code
- DHA04401316902
Company information
- Manufacturer
- PUFF
- Manufacturer Country
- France
- Authorized Representative
- FABRO INTERNATIONAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of dental surgical devices and their accessories (F.6640) under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.6640 Dental surgical devices and accessories thereof
- Import Information
- import
Dates and status
- Registration Date
- Jul 02, 2013
- Expiry Date
- Jul 02, 2018
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Respler" intraoral camera (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c4300775c3c44bd81722013dd977b484 and manufactured by PUFF. The authorized representative in Taiwan is FABRO INTERNATIONAL CO., LTD..
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