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“Martin” E series Surgical Light - Taiwan Registration 7c018d93a9b358f61325cf5e814e1a7d

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 7c018d93a9b358f61325cf5e814e1a7d 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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7c018d93a9b358f61325cf5e814e1a7d
Registration Details
Taiwan FDA Registration: 7c018d93a9b358f61325cf5e814e1a7d
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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

7c018d93a9b358f61325cf5e814e1a7d

Ministry of Health Medical Device Import No. 036745

DHA05603674502

Company Information

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I4580 Surgical light

Imported from abroad

Dates and Status

Sep 25, 2023

Sep 25, 2028

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