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“G.N.S” neoV Diode Laser Family - Taiwan Registration 5ba78f9e19b87baaff85cac1ddd1aad6

Access comprehensive regulatory information for “G.N.S” neoV Diode Laser Family in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5ba78f9e19b87baaff85cac1ddd1aad6 and manufactured by G.N.S neoLaser Ltd. The authorized representative in Taiwan is GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH.

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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5ba78f9e19b87baaff85cac1ddd1aad6
Registration Details
Taiwan FDA Registration: 5ba78f9e19b87baaff85cac1ddd1aad6
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Device Details

“G.N.S” neoV Diode Laser Family
TW: “吉恩司”二極體雷射
Risk Class 2
MD

Registration Details

5ba78f9e19b87baaff85cac1ddd1aad6

Ministry of Health Medical Device Import No. 031028

DHA05603102801

Company Information

Israel

Product Details

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

I General and plastic surgical devices

I4810 Lasers for general surgery, plastic surgery and dermatology

Imported from abroad

Dates and Status

Apr 12, 2018

Apr 12, 2028