"iJURA Vadent" dental hand instruments (unsterilized)
Taiwan·Risk Class 1·Ivoclar Vivadent Manufacturing GmbH;;IVOCLAR VIVADENT AG·Registered May 28, 2019 – May 28, 2024Cancelled- Analysis ID
- 1c72312e0922c6623e3b51fb8139784c
- Customs Code
- DHA09402049206
- Manufacturer Country
- Austria;;Liechtenstein
- Authorized Representative
- BioLaden Consultant Corp.
- 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
- Input;; Contract manufacturing
- Registration Date
- May 28, 2019
- Expiry Date
- May 28, 2024
- Cancellation Date
- Aug 08, 2023
- Status
- Logged out
- Reason
- 自行鍵入
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Access comprehensive regulatory information for "iJURA Vadent" 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 1c72312e0922c6623e3b51fb8139784c and manufactured by Ivoclar Vivadent Manufacturing GmbH;;IVOCLAR VIVADENT AG. The authorized representative in Taiwan is BioLaden Consultant Corp..
This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including Ivoclar Vivadent, Inc.; IVOCLAR VIVADENT AG, IVOCLAR VIVADENT AG;; GEB. RENGGLI AG, and 5 recent registrations in the same category. 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.