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"Kentila" diode laser system - Taiwan Registration 695047b1588ea60de3edc0261ab0b636

Access comprehensive regulatory information for "Kentila" diode laser system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 695047b1588ea60de3edc0261ab0b636 and manufactured by CANDELA CORPORATION. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..

This page provides complete technical specifications, regulatory compliance details. 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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695047b1588ea60de3edc0261ab0b636
Registration Details
Taiwan FDA Registration: 695047b1588ea60de3edc0261ab0b636
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Device Details

"Kentila" diode laser system
TW: "่‚ฏ็ฌฌๆ‹‰" ไบŒๆฅต้ซ”้›ทๅฐ„็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

695047b1588ea60de3edc0261ab0b636

DHA00600988200

Company Information

United States

Product Details

Vacuum.

I General, Plastic Surgery and Dermatology

import

Dates and Status

Apr 19, 2002

Apr 19, 2022

Apr 12, 2024

Cancellation Information

Logged out

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