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"Bionix" Radiologic Patient Cradle (Non-Sterile) - Taiwan Registration cc99c4f0c76ea2b8e6ee7252a76dcaa3

Access comprehensive regulatory information for "Bionix" 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 cc99c4f0c76ea2b8e6ee7252a76dcaa3 and manufactured by BIONIX RADIATION THERAPY. The authorized representative in Taiwan is SSGI TAIWAN CO..

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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cc99c4f0c76ea2b8e6ee7252a76dcaa3
Registration Details
Taiwan FDA Registration: cc99c4f0c76ea2b8e6ee7252a76dcaa3
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Device Details

"Bionix" Radiologic Patient Cradle (Non-Sterile)
TW: "็•ขๆญๅ…งๅ…‹" ๆ”พๅฐ„็ง‘็—…ๆ‚ฃ็”จๆ”ฏๆžถ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

cc99c4f0c76ea2b8e6ee7252a76dcaa3

Ministry of Health Medical Device Import No. 015008

DHA09401500807

Company Information

United States

Product Details

P Devices for radiology

P1830 Stent for radiology patients

Imported from abroad

Dates and Status

Mar 17, 2015

Mar 17, 2020

Jun 16, 2022

Cancellation Information

Logged out

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