iKAR Vita Wadent Dental Hand Instruments (Unsterilized)
Taiwan·Risk Class 1·IVOCLAR VIVADENT, INC·Registered May 24, 2013 – May 24, 2023Cancelled- Analysis ID
- 1046990c4d09421a9124b59fa75e5443
- Customs Code
- DHA04401305309
- Manufacturer
- IVOCLAR VIVADENT, INC
- Manufacturer Country
- Philippines
- Authorized Representative
- MYWAY INTERNATIONAL CO., LTD.
- 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
- Registration Date
- May 24, 2013
- Expiry Date
- May 24, 2023
- Cancellation Date
- Mar 06, 2019
- Status
- Logged out
- Reason
- 自請註銷
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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 1046990c4d09421a9124b59fa75e5443 and manufactured by IVOCLAR VIVADENT, INC. The authorized representative in Taiwan is MYWAY INTERNATIONAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including GEB. BRASSELER GMBH & CO KG;; IVOCLAR VIVADENT AG, 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.