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"LAPLASER" Light Beam Patient Position Indicator (Non-Sterile) - Taiwan Registration 856c7b6c95ee2c3e29dc72248c694acb

Access comprehensive regulatory information for "LAPLASER" 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 856c7b6c95ee2c3e29dc72248c694acb and manufactured by LAPLASER APPLIKATIONEN GMBH. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..

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856c7b6c95ee2c3e29dc72248c694acb
Registration Details
Taiwan FDA Registration: 856c7b6c95ee2c3e29dc72248c694acb
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Device Details

"LAPLASER" Light Beam Patient Position Indicator (Non-Sterile)
TW: "้›ทๆ™ฎ้›ทๅฐ„" ๅ…‰ๆŸ็—…ๆ‚ฃๅฎšไฝๆŒ‡็คบ็‡ˆ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

856c7b6c95ee2c3e29dc72248c694acb

Ministry of Health Medical Device Import No. 017189

DHA09401718908

Company Information

Germany

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

Nov 17, 2016

Nov 17, 2021