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"Lisa" Reflex laser system - Taiwan Registration 2979de80a8bc2a17b86dbba6b5baa79c

Access comprehensive regulatory information for "Lisa" Reflex 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 2979de80a8bc2a17b86dbba6b5baa79c and manufactured by LISA Laser Products GmbH. The authorized representative in Taiwan is REVO LASER CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including LISA Laser Products GmbH, 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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2979de80a8bc2a17b86dbba6b5baa79c
Registration Details
Taiwan FDA Registration: 2979de80a8bc2a17b86dbba6b5baa79c
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Device Details

"Lisa" Reflex laser system
TW: "้บ—ๆฒ™"็‘ž็ฆ้›ทๆ–ฏ้›ทๅฐ„็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

2979de80a8bc2a17b86dbba6b5baa79c

DHA00601747802

Company Information

Germany

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 11, 2006

Dec 11, 2021

Aug 15, 2023

Cancellation Information

Logged out

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