SEARCH RESULTS FOR: (*Imitation Ecole Nationale d*)(2924780 results)

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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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Spacelabs Interface Cable
RETIA MEDICAL, LLC
FG-007
In Commercial Distribution

  • 00860001506464 ()


  • Noninvasive haemodynamic monitoring system
Drager Interface Cable (14-pin MDR)
RETIA MEDICAL, LLC
FG-006
In Commercial Distribution

  • 00860001506457 ()


  • Noninvasive haemodynamic monitoring system
GE Interface Cable (7-pin Mini-DIN)
RETIA MEDICAL, LLC
FG-005
In Commercial Distribution

  • 00860001506440 ()


  • Noninvasive haemodynamic monitoring system
Transducer Interface Cable
RETIA MEDICAL, LLC
FG-004
In Commercial Distribution

  • 00860001506433 ()


  • Noninvasive haemodynamic monitoring system
GE Interface Cable (9-pin PDM)
RETIA MEDICAL, LLC
FG-003
In Commercial Distribution

  • 00860001506426 ()


  • Noninvasive haemodynamic monitoring system
Philips Interface Cable (3.5 mm Stereo Jack)
RETIA MEDICAL, LLC
FG-002
In Commercial Distribution

  • 00860001506419 ()


  • Noninvasive haemodynamic monitoring system
The Argos Cardiac Output monitoring device is intended for use on patients above the age of 18. It is intended to be used as a hemodynamic monitor for monitoring cardiac output and its derived parameters on patients in the intensive care unit or the operating room.
RETIA MEDICAL, LLC
FG-001
In Commercial Distribution

  • 00860001506402 ()


  • Noninvasive haemodynamic monitoring system
No Description
REFLEXION HEALTH, INC.
3.3.2-2.13.0
In Commercial Distribution

  • 00860001498400 ()


  • Virtual-display rehabilitation system, non-supportive, clinical
Also covers the following minor/medium updates: v3.1.0: (01)00860001471731(11)210526(10)310; v3.1.1 (01)00860001471731(11)210604(10)311; v3.1.2 (01)00860001471731(11)210625(10)312; v3.2.0 (01)00860001471731(11)210713(10)320; v3.2.1. (01)00860001471731(11)210804(10)321; v3.2.2 (01)00860001471731(11)210917(10)322; v3.2.3 (01)00860001471731(11)211026(10)323 ;v3.2.4 (01)00860001471731(11)211123(10)324; v3.4.0: (01)00860001471731(11)220609(10)340; v3.5.1 (01)00860001471731(11)220718(10)351; v3.6.0 (01)00860001471731(11)220926(10)360; v3.6.2(01)00860001471731(11)221024(10)362; v3.7.0(01)00860001471731(11)221116(10)370; v3.8.0(01)00860001471731(11)221215(10)380; v3.8.1(01)00860001471731(11)230127(10)381; v3.9.0(01)00860001471731(11)230217(10)390; v3.9.1(01)00860001471731(11)230417(10)391; v3.9.2 (01)00860001471731(11)230609(10)392; v3.9.3 (01)00860001471731(11)230714(10)393; v3.10.0 (01)00860001471731(11)231013(10)3100
AMPLIFON SPA
Android v3
In Commercial Distribution

  • 00860001471731 ()


  • Hearing aid/implant system remote control
Also covers the following minor/medium updates: v3.1.0 (01)00860001471724(11)210526(10)310; v3.1.1 (01)00860001471724(11)210604(10)311; v3.1.2 (01)00860001471724(11)210625(10)312; v3.2.0 (01)00860001471724(11)210713(10)320; v3.2.1. (01)00860001471724(11)210804(10)321; v3.2.2 (01)00860001471724(11)210917(10)322; v3.2.3 (01)00860001471724(11)211026(10)323 ;v3.2.4 (01)00860001471724(11)211123(10)324; v3.7.0 (01)00860001471724(11) 221116(10)370; v3.6.2 (01)00860001471724(11) 221024(10)362; v3.4.0:(01)00860001471724(11)220609(10)350; v3.5.1(01)00860001471724(11)220718(10)351; v3.6.0 (01)00860001471724(11) 220926(10)360; v3.8.0 (01)00860001471724(11) 221215(10)380; v3.8.1 (01)00860001471724(11) 230127(10)381; v3.9.0 (01)00860001471724(11) 230217(10)390; v3.9.1 (01)00860001471724(11) 230417(10)391; v3.9.2 (01)00860001471724(11) 230609(10)392; v3.9.3 (01)00860001471724(11) 230714(10)393; v3.10.0 (01)00860001471724(11) 231013(10)3100
AMPLIFON SPA
iOS v3
In Commercial Distribution

  • 00860001471724 ()


  • Hearing aid/implant system remote control
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