"Straumann" (sterilized) accessories for healing
- Analysis ID
- 1cf3cdf361c17192ff3828340caa9b72
- Customs Code
- DHA05603591901
- Manufacturer
- Straumann Villeret SA;; Institut Straumann AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- Straumann Group (Taiwan) Co. Ltd.
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3630 Bolsters for intraosseous implants
- Import Information
- import
- Registration Date
- Oct 03, 2022
- Expiry Date
- Oct 03, 2027
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Access comprehensive regulatory information for "Straumann" (sterilized) accessories for healing in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1cf3cdf361c17192ff3828340caa9b72 and manufactured by Straumann Villeret SA;; Institut Straumann AG. The authorized representative in Taiwan is Straumann Group (Taiwan) Co. Ltd..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including INSTITUT STRAUMANN AG;; STRAUMANN MADE INC., 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.