Pure Global

“O.R.” Uterine ElevatOR PRO with OccludOR Balloon - Taiwan Registration 0d67d1efd57a4b6dda7f30642849f67b

Access comprehensive regulatory information for “O.R.” Uterine ElevatOR PRO with OccludOR Balloon in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0d67d1efd57a4b6dda7f30642849f67b and manufactured by The OR Company Pty Ltd. The authorized representative in Taiwan is DOUBLE-SUCCESS 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
0d67d1efd57a4b6dda7f30642849f67b
Registration Details
Taiwan FDA Registration: 0d67d1efd57a4b6dda7f30642849f67b
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“O.R.” Uterine ElevatOR PRO with OccludOR Balloon
TW: “歐爾”子宮昇降器(含封堵氣球)
Risk Class 2
MD

Registration Details

0d67d1efd57a4b6dda7f30642849f67b

Ministry of Health Medical Device Import No. 033887

DHA05603388704

Company Information

Australia

Product Details

For details, it is Chinese approved copy of the imitation order

l Devices for obstetrics and gynecology

L4530 Manual instruments for obstetrics and gynecology

Imported from abroad

Dates and Status

Aug 14, 2020

Aug 14, 2025