“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.
Device Details
Registration Details
4c8d2a34bb082186048571bd0ca1cdc2
Ministry of Health Medical Device Import No. 030981
DHA05603098107
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

