"Candulor" Resin impression tray material (Non-Sterile)
Taiwan·Risk Class 1·MD·CANDULOR AG·Registered Oct 01, 2021 – Oct 31, 2026Active- Analysis ID
- a3fa0b2276cc6a8ab7e0b68487050a2b
- License Form
- Ministry of Health Medical Device Import Registration No. 022430
- Customs Code
- DHA08402243001
- Manufacturer
- CANDULOR AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- GOETHE BIOTECH CO., LTD.
- Intended Use
- Limited to the first level identification range of resin impression dental tray (F.3670) of the management method for medical equipment.
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3670 resin impression dental tray
- Import Information
- Imported from abroad
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
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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 a3fa0b2276cc6a8ab7e0b68487050a2b 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.