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“Martin” E Series Surgical Light - Taiwan Registration 4c8d2a34bb082186048571bd0ca1cdc2

Access comprehensive regulatory information for “Martin” E Series Surgical Light in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4c8d2a34bb082186048571bd0ca1cdc2 and manufactured by GEBRUDER MARTIN GMBH & CO. KG. The authorized representative in Taiwan is KINDMED CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GEBRUDER MARTIN GMBH & 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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4c8d2a34bb082186048571bd0ca1cdc2
Registration Details
Taiwan FDA Registration: 4c8d2a34bb082186048571bd0ca1cdc2
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Device Details

“Martin” E Series Surgical Light
TW: “瑪珽” E系列手術燈
Risk Class 2
MD

Registration Details

4c8d2a34bb082186048571bd0ca1cdc2

Ministry of Health Medical Device Import No. 030981

DHA05603098107

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

I General and plastic surgical devices

I4580 Surgical light

Imported from abroad

Dates and Status

Mar 15, 2018

Mar 15, 2023

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