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"Kellos Martin" electrode - Taiwan Registration c55552297f9f09748df5554a8929aa33

Access comprehensive regulatory information for "Kellos Martin" electrode in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c55552297f9f09748df5554a8929aa33 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 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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c55552297f9f09748df5554a8929aa33
Registration Details
Taiwan FDA Registration: c55552297f9f09748df5554a8929aa33
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Device Details

"Kellos Martin" electrode
TW: โ€œๅ‡ฑๆจ‚ๆ€้ฆฌไธโ€้›ป็‡’้›ปๆฅต
Risk Class 2

Registration Details

c55552297f9f09748df5554a8929aa33

DHA05603548405

Company Information

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I.4400 Cutting and hemostasis electric knives and accessories thereof

import

Dates and Status

May 24, 2022

May 24, 2027

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