Taiwan FDA registration dad26a7be16f30884b68145216bb5959
"Vityda" dental root canal file (unsterilized)
TW: “威帝達”牙科根管銼（未滅菌）
Taiwan·Risk Class 1·VDW GMBH·Registered Dec 16, 2010 – Dec 16, 2015CancelledRegistration details
- Analysis ID
- dad26a7be16f30884b68145216bb5959
- Customs Code
- DHA04400969100
Company information
- Manufacturer
- VDW GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Taiwan Branch of American Denspie 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
- Dec 16, 2010
- Expiry Date
- Dec 16, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Vityda" dental root canal file (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dad26a7be16f30884b68145216bb5959 and manufactured by VDW GMBH. The authorized representative in Taiwan is Taiwan Branch of American Denspie Co., Ltd.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices