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"CDR" Radiologic Patient Cradle (Non-Sterile) - Taiwan Registration ef2f33f065a65969a9bd6f75cd6340f4

Access comprehensive regulatory information for "CDR" Radiologic Patient Cradle (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ef2f33f065a65969a9bd6f75cd6340f4 and manufactured by CDR Systems Inc.. The authorized representative in Taiwan is Yaukang international 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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ef2f33f065a65969a9bd6f75cd6340f4
Registration Details
Taiwan FDA Registration: ef2f33f065a65969a9bd6f75cd6340f4
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Device Details

"CDR" Radiologic Patient Cradle (Non-Sterile)
TW: "ๅธŒ่ฟช็ˆพ"ๆ”พๅฐ„็ง‘็—…ๆ‚ฃ็”จๆ”ฏๆžถ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

ef2f33f065a65969a9bd6f75cd6340f4

Ministry of Health Medical Device Import No. 020403

DHA09402040307

Company Information

Canada

Product Details

Limited to the first-level identification range of the Measures for the Administration of Medical Equipment "Stent for Radiology Patients (P.1830)".

P Devices for radiology

P1830 Stent for radiology patients

Imported from abroad

Dates and Status

May 06, 2019

May 06, 2024