Pure Global

"Bolema" pulsed light and laser system - Taiwan Registration 1e17a621b0495de0e58ab006612d1131

Access comprehensive regulatory information for "Bolema" pulsed light and 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 1e17a621b0495de0e58ab006612d1131 and manufactured by PALOMAR MEDICAL TECHNOLOGIES, INC.. 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
1e17a621b0495de0e58ab006612d1131
Registration Details
Taiwan FDA Registration: 1e17a621b0495de0e58ab006612d1131
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Bolema" pulsed light and laser system
TW: "ๅฏถๆจ‚็‘ช"่„ˆ่กๅ…‰ๅŠ้›ทๅฐ„็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

1e17a621b0495de0e58ab006612d1131

DHA00601687201

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

I General, Plastic Surgery and Dermatology

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

import

Dates and Status

Jul 12, 2006

Jul 12, 2016

May 25, 2018

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ