"Straumann" (sterilized) accessories for healing
- Analysis ID
- 222c1e91b621b5b7fe97bdf0bd5f39d8
- Customs Code
- DHA05603413909
- Manufacturer
- INSTITUT STRAUMANN AG;; STRAUMANN MADE INC.
- Manufacturer Country
- United States;;Switzerland
- Authorized Representative
- Straumann Group (Taiwan) Co. Ltd.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3630 Bolsters for intraosseous implants
- Import Information
- import
- Registration Date
- Jan 02, 2021
- Expiry Date
- Jan 02, 2026
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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 222c1e91b621b5b7fe97bdf0bd5f39d8 and manufactured by INSTITUT STRAUMANN AG;; STRAUMANN MADE INC.. 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 Straumann Villeret SA;; Institut Straumann 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.