iKAR Vita Wadent Dental Hand Instruments (Unsterilized)
Taiwan·Risk Class 1·GEB. BRASSELER GMBH & CO KG;; IVOCLAR VIVADENT AG·Registered Dec 16, 2009 – Dec 16, 2024Expired- Analysis ID
- 8a41eb1b1c18394bc79d3447e91e94b3
- Customs Code
- DHA04400839606
- Manufacturer Country
- Liechtenstein;;Germany
- 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
- Dec 16, 2009
- Expiry Date
- Dec 16, 2024
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Access comprehensive regulatory information for iKAR Vita Wadent 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 8a41eb1b1c18394bc79d3447e91e94b3 and manufactured by GEB. BRASSELER GMBH & CO KG;; IVOCLAR VIVADENT AG. The authorized representative in Taiwan is BioLaden Consultant Corp..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including IVOCLAR VIVADENT, INC, IVOCLAR VIVADENT AG, and 2 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.