"iJURA Vadent" dental hand instruments (unsterilized)
Taiwan·Risk Class 1·IVOCLAR VIVADENT AG;; GEB. RENGGLI AG·Registered Apr 03, 2019 – Apr 03, 2029Active- Analysis ID
- 1f31230f2209540b47daf7708bcab181
- Customs Code
- DHA09402027001
- Manufacturer
- IVOCLAR VIVADENT AG;; GEB. RENGGLI AG
- Manufacturer Country
- Liechtenstein;;Switzerland
- Authorized Representative
- BioLaden Consultant Corp.
- Intended Use
- Limited to the classification and grading management of medical equipment, the first level identification range of 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
- Contract manufacturing;; input
- Registration Date
- Apr 03, 2019
- Expiry Date
- Apr 03, 2029
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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 1f31230f2209540b47daf7708bcab181 and manufactured by IVOCLAR VIVADENT AG;; GEB. RENGGLI 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;; Helmut Zepf Medizintechnik GmbH, 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.