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“MEDRAD” Qwik Fit Syringe - Taiwan Registration 0cae007c1f117d7ea9db4ce1bce6971d

Access comprehensive regulatory information for “MEDRAD” Qwik Fit Syringe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0cae007c1f117d7ea9db4ce1bce6971d and manufactured by Bayer Medical Care Inc.. The authorized representative in Taiwan is HSIEN TAI 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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0cae007c1f117d7ea9db4ce1bce6971d
Registration Details
Taiwan FDA Registration: 0cae007c1f117d7ea9db4ce1bce6971d
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Device Details

“MEDRAD” Qwik Fit Syringe
TW: “美樂得”注射筒組套
Risk Class 2
MD

Registration Details

0cae007c1f117d7ea9db4ce1bce6971d

Ministry of Health Medical Device Import No. 027859

DHA05602785900

Company Information

United States

Product Details

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

E Cardiovascular devices

E1650 Vascular photography syringes and syringes

Imported from abroad

Dates and Status

Nov 26, 2015

Nov 26, 2025