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"Kellos Martin" electrosurgical system - Taiwan Registration 891b780100449abda68d018f876ab10f

Access comprehensive regulatory information for "Kellos Martin" electrosurgical system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 891b780100449abda68d018f876ab10f and manufactured by KLS MARTIN SE & CO. KG;; KLS Martin SE & Co. KG. The authorized representative in Taiwan is KLS MARTIN TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including KLS MARTIN SE & CO. KG;; KLS Martin SE & Co. KG, and 2 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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891b780100449abda68d018f876ab10f
Registration Details
Taiwan FDA Registration: 891b780100449abda68d018f876ab10f
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Device Details

"Kellos Martin" electrosurgical system
TW: โ€œๅ‡ฑๆจ‚ๆ€้ฆฌไธโ€้›ปๅˆ€็ณป็ตฑ
Risk Class 2

Registration Details

891b780100449abda68d018f876ab10f

DHA05603414201

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

Jan 03, 2021

Jan 03, 2026

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