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"Lominnis" Aluma Wave Tightening System - Taiwan Registration f38e565236a5fae56a584a5029699463

Access comprehensive regulatory information for "Lominnis" Aluma Wave Tightening System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f38e565236a5fae56a584a5029699463 and manufactured by LUMENIS LTD.. The authorized representative in Taiwan is Taiwan Branch of Hong Kong Commercial Medical Laser Co., 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.

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f38e565236a5fae56a584a5029699463
Registration Details
Taiwan FDA Registration: f38e565236a5fae56a584a5029699463
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Device Details

"Lominnis" Aluma Wave Tightening System
TW: โ€œๆด›ๆ˜Žๅฐผๆ–ฏโ€ๆ„›้œฒ็‘ช้›ปๆณข็ทŠ่†š็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

f38e565236a5fae56a584a5029699463

DHA00601883505

Company Information

Product Details

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

I General, Plastic Surgery and Dermatology

I.4400 Cutting and hemostasis electric knives and accessories thereof

import

Dates and Status

May 01, 2008

May 01, 2013

Aug 13, 2015

Cancellation Information

Logged out

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