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Greenever Light Beam Patient Position Indicator (Non-Sterile) - Taiwan Registration 0ba6951a29cc9db03a3e5ded62602bbe

Access comprehensive regulatory information for Greenever Light Beam Patient Position Indicator (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 0ba6951a29cc9db03a3e5ded62602bbe and manufactured by CEDAR ELECTRO INC.. The authorized representative in Taiwan is GREENEVER MEDICAL SYSTEMS INC ..

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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0ba6951a29cc9db03a3e5ded62602bbe
Registration Details
Taiwan FDA Registration: 0ba6951a29cc9db03a3e5ded62602bbe
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Device Details

Greenever Light Beam Patient Position Indicator (Non-Sterile)
TW: ๅธธๆท ็—…ๆ‚ฃๅฎšไฝๅ…‰ๆŸๆŒ‡็คบๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

0ba6951a29cc9db03a3e5ded62602bbe

Ministry of Health Medical Device Import No. 019540

DHA09401954004

Company Information

Canada

Product Details

Limited to the first level recognition range of the Measures for the Administration of Medical Equipment "Patient Positioning Beam Indicator (P.5780)".

P Devices for radiology

P5780 Patient Positioning Beam Indicator

Imported from abroad

Dates and Status

Aug 23, 2018

Aug 23, 2023