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"Kellos Martin" bipolar electrofired instrument - Taiwan Registration f8ae55fbb07c548f7fb1b6bb603f32f2

Access comprehensive regulatory information for "Kellos Martin" bipolar electrofired instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f8ae55fbb07c548f7fb1b6bb603f32f2 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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f8ae55fbb07c548f7fb1b6bb603f32f2
Registration Details
Taiwan FDA Registration: f8ae55fbb07c548f7fb1b6bb603f32f2
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Device Details

"Kellos Martin" bipolar electrofired instrument
TW: โ€œๅ‡ฑๆจ‚ๆ€้ฆฌไธโ€้›™ๆฅต้›ป็‡’ๅ™จๆขฐ
Risk Class 2

Registration Details

f8ae55fbb07c548f7fb1b6bb603f32f2

DHA05603285206

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

Sep 27, 2019

Sep 27, 2029

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