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“MEDRAD” Disposable Syringe Kit - Taiwan Registration c9fb884625ff0f52e2bcf906d1d08087

Access comprehensive regulatory information for “MEDRAD” Disposable Syringe Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c9fb884625ff0f52e2bcf906d1d08087 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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c9fb884625ff0f52e2bcf906d1d08087
Registration Details
Taiwan FDA Registration: c9fb884625ff0f52e2bcf906d1d08087
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Device Details

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

Registration Details

c9fb884625ff0f52e2bcf906d1d08087

Ministry of Health Medical Device Import No. 027874

DHA05602787409

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

Dec 11, 2015

Dec 11, 2025