"Kentila" pulsed dye laser
- Analysis ID
- a77c71b84155fae45a77530a0e8ebedc
- Customs Code
- DHA00601162702
- Manufacturer
- CANDELA LASER CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- DYNAMIC MEDICAL TECHNOLOGIES INC.
- Intended Use
- It is used to treat skin or vascular lesions such as localized plaques, scars, hemangiomas, and wine-colored spots.
- 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
- import
- Registration Date
- Jul 26, 2005
- Expiry Date
- Jul 26, 2010
- Cancellation Date
- Nov 01, 2012
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Kentila" pulsed dye laser in Taiwan's medical device market through Pure Global AI's free database. is registered under number a77c71b84155fae45a77530a0e8ebedc and manufactured by CANDELA LASER CORPORATION. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Valtronic Technologies (Suisse) SA;; Candela Corporation, 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.