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"Kentila" pulsed dye laser - Taiwan Registration a77c71b84155fae45a77530a0e8ebedc

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.

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a77c71b84155fae45a77530a0e8ebedc
Registration Details
Taiwan FDA Registration: a77c71b84155fae45a77530a0e8ebedc
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Device Details

"Kentila" pulsed dye laser
TW: "่‚ฏ็ฌฌๆ‹‰" ่„ˆ่กๅผๆŸ“ๆ–™้›ทๅฐ„
Cancelled

Registration Details

a77c71b84155fae45a77530a0e8ebedc

DHA00601162702

Company Information

United States

Product Details

It is used to treat skin or vascular lesions such as localized plaques, scars, hemangiomas, and wine-colored spots.

I General, Plastic Surgery and Dermatology

I.4810 Lasers for general surgical, orthopaedic and dermatological use

import

Dates and Status

Jul 26, 2005

Jul 26, 2010

Nov 01, 2012

Cancellation Information

Logged out

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