"DORNIER" diode laser
Taiwan·Risk Class 2·Dornier MedTech America, Inc.; DORNIER MEDTECH SYSTEMS GMBH·Registered Apr 15, 2008 – Apr 15, 2028Active- Analysis ID
- 513d85d111c6e586f0e8f722f3aba3b2
- Customs Code
- DHA00601879404
- Manufacturer Country
- United States;;Germany
- Authorized Representative
- MEDEN INTERNATIONAL INC.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4810 Lasers for general surgical, orthopaedic and dermatological use
- Import Information
- Contract manufacturing;; input
- Registration Date
- Apr 15, 2008
- Expiry Date
- Apr 15, 2028
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Access comprehensive regulatory information for "DORNIER" diode laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 513d85d111c6e586f0e8f722f3aba3b2 and manufactured by Dornier MedTech America, Inc.; DORNIER MEDTECH SYSTEMS GMBH. The authorized representative in Taiwan is MEDEN INTERNATIONAL INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Dornier MedTech America, 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.