"Candulor" Resin impression tray material (Non-Sterile)
Taiwan·Risk Class 1·MD·CANDULOR AG·Registered Mar 31, 2021 – Mar 31, 2026Cancelled- Analysis ID
- 723d0a80904c0f9f9aa1c2e6cb0cfa27
- License Form
- Ministry of Health Medical Device Import No. 022430
- Customs Code
- DHA09402243007
- Manufacturer
- CANDULOR AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- GOETHE BIOTECH CO., LTD.
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3670 resin impression dental tray
- Import Information
- Imported from abroad
- Registration Date
- Mar 31, 2021
- Expiry Date
- Mar 31, 2026
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for "Candulor" Resin impression tray material (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 723d0a80904c0f9f9aa1c2e6cb0cfa27 and manufactured by CANDULOR AG. The authorized representative in Taiwan is GOETHE BIOTECH CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CANDULOR 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.