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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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KermaX-plus - EIBA120131250

KermaX Product family is designed to be installed in diagnostic x-ray units and is intended to be used for the measurement of Dose Area Product (DAP)/ DAP rate, exposure time.
IBA Dosimetry GmbH
1
In Commercial Distribution

  • EIBA120131251 ()
  • EIBA120131250 ()
120-131ZKCANO

  • Diagnostic x-ray system quality assurance device

KermaX-plus - EIBA120131240

KermaX Product family is designed to be installed in diagnostic x-ray units and is intended to be used for the measurement of Dose Area Product (DAP)/ DAP rate, exposure time.
IBA Dosimetry GmbH
4
In Commercial Distribution

  • EIBA120131241 ()
  • EIBA120131240 ()
120-131OEM CAN

  • Diagnostic x-ray system quality assurance device

B.R.A.H.M.S KRYPTOR BUFFER - 04260157638990

No Description
B.R.A.H.M.S GmbH
89970
In Commercial Distribution

  • 04260157638990 ()


  • Fluorescent immunoassay analyser IVD, laboratory

B.R.A.H.M.S KRYPTOR compact DILCUP - 04260157638983

No Description
B.R.A.H.M.S GmbH
89985
In Commercial Distribution

  • 04260157638983 ()


  • Fluorescent immunoassay analyser IVD, laboratory

B.R.A.H.M.S KRYPTOR compact REACT - 04260157638976

No Description
B.R.A.H.M.S GmbH
89986
In Commercial Distribution

  • 04260157638976 ()


  • Fluorescent immunoassay analyser IVD, laboratory

B.R.A.H.M.S KRYPTOR compact PLUS - 04260157630949

No Description
B.R.A.H.M.S GmbH
106172
In Commercial Distribution

  • 04260157630949 ()


  • Fluorescent immunoassay analyser IVD, laboratory

ATLAS Corneal Topography System - 04057748081118

The ZEISS ATLAS Corneal Topography System is intended to measure and analyze the corneal curvature of the eye.
Carl Zeiss Meditec, Inc.
9000
Not in Commercial Distribution

  • 04057748081118 ()


  • Corneal topography system

FeetMe Monitor FTM-DK - 03760349820055

No Description
FEETME
PVT3
In Commercial Distribution

  • 03760349820093 ()
  • 03760349820055 ()
  • 03760349820048 ()


  • Pressure monitoring insole

FeetMe Monitor FTM-DK - 03760349820048

FeetMe Monitor Medical device corresponding to a pair of connected insoles Model FTM-DK and version PVT2
FEETME
PVT2
In Commercial Distribution

  • 03760349820086 ()
  • 03760349820048 ()

  • EU-36
  • EU-35
  • EU-37
  • EU-38
  • EU-39
  • EU-40
  • EU-41
  • EU-42
  • EU-43
  • EU-44
  • EU-45
  • EU-46


  • Pressure monitoring insole

FeetMe Monitor FTM-DK - 03760349820000

Medical device corresponding to a pair of connected insoles model FTM-DK, version PVT1
FEETME
PVT1
In Commercial Distribution

  • 03760349820000 ()
  • 03760349820079 ()

  • EU-41
  • EU-35
  • EU-36
  • EU-37
  • EU-38
  • EU-39
  • EU-40
  • EU-42
  • EU-43
  • EU-46
  • EU-44
  • EU-45


  • Pressure monitoring insole
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