Retiro De Equipo (Recall) de Device Recall GE Healthcare Precision 500D

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83098669808 00000096516HL0 83090416600 00000101667HL4 83093535827 00000080557HL2 613969RF1 00000094745HL7 416323RAD2 00000087234HL1 M1797703 00000101659HL1 IE1006WD01 00000085227HL7 A5805631 00000096517HL8 JO1034RX08 00000079664HL9 RO1096XR01 00000081031HL7 RO1096XR01 00000091661HL9 RU1279RX03 00000080195HL1 AE1021RX04 00000077641HL9 00141RAD05 00000080193HL6 10670WDR01 00000084555HL2 00313WDR01 00000084988HL5 00100WDR02 00000089178HL8 00618RAD01 00000094998HL2 00254RAD01 00000095388HL5 05528WDR01 00000101665HL8 IE1564RX03

Radiology Devices

2

No

Worldwide Distribution - USA (nationwide) including the states of AL, AK, AZ, AR, CA, CO, DC, FL. GA, HI. IA, ID, IL, IN, LA, KY, ME, MD, MA, MI, MN, MS, MO, NE, NV, NH, NJ, NM, NY, NC, OH, OK, OR, PA, TN ,KY, TX, UT, VA, WA, WV, WI and WY., and the countries of ARGENTINA, AUSTRALIA, CANADA, FRANCE, IRELAND, ITALY, JORDAN, ROMANIA, RUSSIA, UNITED ARAB EMIRATES and UNITED KINGDOM.

GE Healthcare Precision 500D and Proteus XR/a equipped with Wireless Digital Radiography Option (WDR1). || The Wireless DR Imaging Option ( WDR1), when used with a radiographic imaging system, is indicted for use in general radiographic images of human anatomy. It is intended for use in all routine radiography exams, and specialized areas including pediatric work, intensive care and trauma, wherever conventional screen-film systems or CR systems may be used. The device is not intended for mammography or fluoroscopy applications.