"Vericom" EDTA Root Canal Preparator (Non-Sterile)
Taiwan·Risk Class 1·MD·VERICOM CO., LTD.·Registered May 04, 2017 – May 04, 2027Active- Analysis ID
- 005d86be3434f3042b4e051a058d444b
- License Form
- Ministry of Health Medical Device Import No. 017788
- Customs Code
- DHA09401778804
- Manufacturer
- VERICOM CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- SUNDENT CORPORATION
- 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 Dental devices
- Product Type (Level 2)
- F4565 Hand instruments for dental use
- Import Information
- Imported from abroad
- Registration Date
- May 04, 2017
- Expiry Date
- May 04, 2027
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Access comprehensive regulatory information for "Vericom" EDTA Root Canal Preparator (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 005d86be3434f3042b4e051a058d444b and manufactured by VERICOM CO., LTD.. The authorized representative in Taiwan is SUNDENT CORPORATION.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including VERICOM CO., LTD., and 1 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.