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"Kelis Martin" bipolar sealed instrument - Taiwan Registration 6e140ba164f8d43e315dffeae185df4d

Access comprehensive regulatory information for "Kelis Martin" bipolar sealed instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6e140ba164f8d43e315dffeae185df4d 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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6e140ba164f8d43e315dffeae185df4d
Registration Details
Taiwan FDA Registration: 6e140ba164f8d43e315dffeae185df4d
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Device Details

"Kelis Martin" bipolar sealed instrument
TW: โ€œๅ‡ฑๆจ‚ๆ€้ฆฌไธโ€้›™ๆฅตๅฏ†ๅฐๅ™จๆขฐ
Risk Class 2

Registration Details

6e140ba164f8d43e315dffeae185df4d

DHA05603156307

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

Aug 20, 2018

Aug 20, 2028

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