Pure Global

"New Nalon" e laser system - Taiwan Registration 27621cfe969ffc0f9ce930a166752554

Access comprehensive regulatory information for "New Nalon" e 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 27621cfe969ffc0f9ce930a166752554 and manufactured by SYNERON MEDICAL LTD.. The authorized representative in Taiwan is LYRA LTD..

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
27621cfe969ffc0f9ce930a166752554
Registration Details
Taiwan FDA Registration: 27621cfe969ffc0f9ce930a166752554
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"New Nalon" e laser system
TW: "ๆ–ฐ้‚ฃ้š†"e้›ทๅฐ„็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

27621cfe969ffc0f9ce930a166752554

DHA00601763900

Company Information

Israel

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

Dec 28, 2006

Dec 28, 2016

Aug 21, 2018

Cancellation Information

Logged out

ๆœชๅฑ•ๅปถ่€Œ้€พๆœŸ่€