Taiwan FDA registration 7c018d93a9b358f61325cf5e814e1a7d

“Martin” E series Surgical Light

TW: “瑪珽”E系列手術燈
Taiwan flagTaiwan·Risk Class 2·MD·GEBRUDER MARTIN GMBH & CO. KG·Registered Sep 25, 2023 – Sep 25, 2028Active
Registration details
Analysis ID
7c018d93a9b358f61325cf5e814e1a7d
License Form
Ministry of Health Medical Device Import No. 036745
Customs Code
DHA05603674502
Company information
Manufacturer Country
Germany
Authorized Representative
KINDMED CORPORATION
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I4580 Surgical light
Import Information
Imported from abroad
Dates and status
Registration Date
Sep 25, 2023
Expiry Date
Sep 25, 2028
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About this record

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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