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“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.

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d19fe1ff5df732650c936e7af71bef53
Registration Details
Taiwan FDA Registration: d19fe1ff5df732650c936e7af71bef53
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Device Details

“GIMMI” Alphaduolap Insufflator
TW: “吉米”阿爾法杜樂普腹腔鏡灌入器
Risk Class 2
MD
Cancelled

Registration Details

d19fe1ff5df732650c936e7af71bef53

Ministry of Health Medical Device Import No. 027839

DHA05602783907

Company Information

Germany

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

Logged out

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