Taiwan FDA registration 98e52fdbc42c1c5c87103acff0f2c1e4
"Pipeden" dental hand instruments (unsterilized)
TW: “派普登”牙科手用器械 (未滅菌)
Taiwan·Risk Class 1·PULPDENT CORPORATION·Registered Jun 18, 2013 – Jun 18, 2018CancelledRegistration details
- Analysis ID
- 98e52fdbc42c1c5c87103acff0f2c1e4
- Customs Code
- DHA04401311607
Company information
- Manufacturer
- PULPDENT CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- Yourun Dental Materials Co., Ltd
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
- Jun 18, 2013
- Expiry Date
- Jun 18, 2018
- Cancellation Date
- Nov 28, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Pipeden" dental hand instruments (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 98e52fdbc42c1c5c87103acff0f2c1e4 and manufactured by PULPDENT CORPORATION. The authorized representative in Taiwan is Yourun Dental Materials Co., Ltd.
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