"iJURA Vadent" resin applicator (unsterilized)
Taiwan·Risk Class 1·IVOCLAR VIVADENT INC. (IVPH);;IVOCLAR VIVADENT AG·Registered Oct 01, 2021 – Oct 31, 2023Cancelled- Analysis ID
- 5841e3858d3e628a0b3c3850ac3c10ed
- Customs Code
- DHA08401910707
- Manufacturer Country
- Philippines;;Liechtenstein
- Authorized Representative
- BioLaden Consultant Corp.
- Intended Use
- Limited to the first level identification range of resin applicator (F.3140) of the classification and grading management method of medical equipment.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3140 Resin Coating Machine
- Import Information
- Input;; Contract manufacturing
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2023
- Cancellation Date
- Nov 02, 2023
- Status
- Logged out
- Reason
- 未展延而逾期者
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Access comprehensive regulatory information for "iJURA Vadent" resin applicator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5841e3858d3e628a0b3c3850ac3c10ed and manufactured by IVOCLAR VIVADENT INC. (IVPH);;IVOCLAR VIVADENT AG. The authorized representative in Taiwan is BioLaden Consultant Corp..
This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including IVOCLAR VIVADENT INC. (IVPH);;IVOCLAR VIVADENT AG, IVOCLAR VIVADENT AG, and 3 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.