"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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Device Details
Registration Details
856c7b6c95ee2c3e29dc72248c694acb
Ministry of Health Medical Device Import No. 017189
DHA09401718908
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

