Taiwan FDA registration 4c8d2a34bb082186048571bd0ca1cdc2

“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 Mar 15, 2018 – Mar 15, 2023Expired
Registration details
Analysis ID
4c8d2a34bb082186048571bd0ca1cdc2
License Form
Ministry of Health Medical Device Import No. 030981
Customs Code
DHA05603098107
Company information
Manufacturer Country
Germany
Authorized Representative
KINDMED CORPORATION
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
I General and plastic surgical devices
Product Type (Level 2)
I4580 Surgical light
Import Information
Imported from abroad
Dates and status
Registration Date
Mar 15, 2018
Expiry Date
Mar 15, 2023
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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 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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