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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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AMF Revision TT Cones - TT REV CONE Central Femur Dia. 24 mm
LIMACORPORATE SPA
6C10.14.240
In Commercial Distribution

  • 08033390180719 ()

  • Dia. 24 mm
6C10.14.240

  • Sleeve femoral/tibial extension, coated
AMF Revision TT Cones - TT REV CONE Tibia Dia.24 mm
LIMACORPORATE SPA
6C20.14.240
In Commercial Distribution

  • 08033390175913 ()

  • Dia.24 mm
6C20.14.240

  • Sleeve femoral/tibial extension, coated
P24BKN 24G PENCAN TRAY W/BUP & DEX NRFIT
B. BRAUN MEDICAL INC.
339181
In Commercial Distribution

  • 04046964941290 ()
  • 04046964941283 ()

  • Gauge (cannula) : 24
339181

  • Intrathecal anaesthesia set, non-medicated
SSK ADVENTHEALTH ORLANDO
B. BRAUN MEDICAL INC.
560675
In Commercial Distribution

  • 04046955672004 ()
  • 04046955672011 ()

  • Gauge (cannula) : 24
560675

  • Intrathecal anaesthesia set, medicated
Stimuplex® A, 24 Ga. x 1 in. (25 mm) Insulated Needle with 30° Bevel and Extension Set
B. BRAUN MEDICAL INC.
4894251
In Commercial Distribution

  • 04022495101167 ()
  • 04022495101150 ()

  • Gauge (cannula) : 24
4894251

  • Peripheral nerve-block blunt needle
No Description
Zimmer, Inc.
5220-80
In Commercial Distribution

  • 00889024187887 ()

  • 24 mm Diameter
  • Length: 75 Millimeter
00-5220-080-00

  • Knee femur stem prosthesis
No Description
Biomet Orthopedics, LLC
110050024
In Commercial Distribution

  • 00887868571756 ()

  • Size 24 Liner
110050024

  • Acetabular shell
Versa-Kath® with Small Bore Connector 21g x 24"
EPIMED INTERNATIONAL, INC
159-2124
In Commercial Distribution

  • 10818788023565 ()
  • 00818788023568 ()

  • 21g
  • 24 [in_i]
  • Length: 24 Inch
  • Catheter Gauge: 2.4 French
159-2124

  • Epidural anaesthesia set, non-medicated
The AURAGEN™ Cortical Surface Electrodes are designed for intraoperative monitoring of cortical electrical activity in order to define the location of epileptogenic foci. They are placed on the exposed cortical surface or inserted into the subdural space to contact the cortical surface. Cortical Electrodes are available with platinum contacts and vary in size according to the number of contacts. The type of cortical electrode used is dependent on the procedure and the size of area being tested.
INTEGRA NEUROSCIENCES IMPLANT (FRANCE)
AU6X2P2CD
Not in Commercial Distribution

  • M272AU6X2P2CD1 ()
  • 10381780036470 ()

  • 24 platinum contacts


  • Cortical electrode
The AURAGEN™ Cortical Surface Electrodes are designed for intraoperative monitoring of cortical electrical activity in order to define the location of epileptogenic foci. They are placed on the exposed cortical surface or inserted into the subdural space to contact the cortical surface. Cortical Electrodes are available with platinum contacts and vary in size according to the number of contacts. The type of cortical electrode used is dependent on the procedure and the size of area being tested.
INTEGRA NEUROSCIENCES IMPLANT (FRANCE)
AU4X6P2
Not in Commercial Distribution

  • M272AU4X6P21 ()
  • 10381780036388 ()

  • 24 platinum contacts


  • Cortical electrode
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