“GIMMI” Alphaduolap Insufflator - Taiwan Registration d19fe1ff5df732650c936e7af71bef53
Access comprehensive regulatory information for “GIMMI” Alphaduolap Insufflator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d19fe1ff5df732650c936e7af71bef53 and manufactured by GIMMI GMBH. The authorized representative in Taiwan is BEAMED INSTRUMENTS CO., LTD..
This page provides complete technical specifications, regulatory compliance details. 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
d19fe1ff5df732650c936e7af71bef53
Ministry of Health Medical Device Import No. 027839
DHA05602783907
Product Details
l Devices for obstetrics and gynecology
L1730 Laparoscopic perfusion device
Imported from abroad
Dates and Status
Nov 03, 2015
Nov 03, 2020
Dec 07, 2020
Cancellation Information
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