Taiwan FDA registration f8ae55fbb07c548f7fb1b6bb603f32f2

"Kellos Martin" bipolar electrofired instrument

TW: “凱樂思馬丁”雙極電燒器械
Taiwan flagTaiwan·Risk Class 2·KLS MARTIN SE & CO. KG;; KLS Martin SE & Co. KG·Registered Sep 27, 2019 – Sep 27, 2029Active
Registration details
Analysis ID
f8ae55fbb07c548f7fb1b6bb603f32f2
Customs Code
DHA05603285206
Company information
Manufacturer Country
Germany
Authorized Representative
KLS MARTIN TAIWAN LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4400 Cutting and hemostasis electric knives and accessories thereof
Import Information
import
Dates and status
Registration Date
Sep 27, 2019
Expiry Date
Sep 27, 2029
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About this record

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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