"Candulor" Dental hand instrument (Non-sterile)
Taiwan·Risk Class 1·MD·CANDULOR AG·Registered Mar 31, 2021 – Mar 31, 2026Expired- Analysis ID
- de5199df63cf949585a383bcac7e69fe
- License Form
- Ministry of Health Medical Device Import No. 022429
- Customs Code
- DHA09402242909
- Manufacturer
- CANDULOR AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- GOETHE BIOTECH 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 Dental devices
- Product Type (Level 2)
- F4565 Hand instruments for dental use
- Import Information
- Imported from abroad
- Registration Date
- Mar 31, 2021
- Expiry Date
- Mar 31, 2026
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Access comprehensive regulatory information for "Candulor" Dental hand instrument (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 de5199df63cf949585a383bcac7e69fe 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 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.