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"Medspira" Radiologic patient cradle (Non-Sterile) - Taiwan Registration 293b81036d39aff8a5893d5e939fba05

Access comprehensive regulatory information for "Medspira" 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 293b81036d39aff8a5893d5e939fba05 and manufactured by MEDSPIRA LLC. The authorized representative in Taiwan is Meide Medical Devices 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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293b81036d39aff8a5893d5e939fba05
Registration Details
Taiwan FDA Registration: 293b81036d39aff8a5893d5e939fba05
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Device Details

"Medspira" Radiologic patient cradle (Non-Sterile)
TW: "็พŽๅพทๆ–ฏ" ๆ”พๅฐ„็ง‘็—…ๆ‚ฃ็”จๆ”ฏๆžถ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

293b81036d39aff8a5893d5e939fba05

Ministry of Health Medical Device Import No. 014830

DHA09401483001

Company Information

United States

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

Jan 08, 2015

Jan 08, 2025