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“KERA HARVEST” Diode Laser System - Taiwan Registration 1331b0324168a228b94669c1f24f7c83

Access comprehensive regulatory information for “KERA HARVEST” Diode 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 1331b0324168a228b94669c1f24f7c83 and manufactured by KERA HARVEST INCORPORATION. The authorized representative in Taiwan is KERA HARVEST INCORPORATION.

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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1331b0324168a228b94669c1f24f7c83
Registration Details
Taiwan FDA Registration: 1331b0324168a228b94669c1f24f7c83
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Device Details

“KERA HARVEST” Diode Laser System
TW: “成果”二極體雷射系統
Risk Class 2
MD

Registration Details

1331b0324168a228b94669c1f24f7c83

Ministry of Health Medical Device Manufacturing No. 004238

Company Information

Taiwan, Province of China

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

Produced in Taiwan, China

Dates and Status

Nov 28, 2013

Nov 28, 2023