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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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Laerdal System Case, Rigid, FR3
PHILIPS ELECTRONICS NORTH AMERICA CORPORATION
FR3 System Case, Ridge
Not in Commercial Distribution

  • 00884838055711 ()
989803157531

  • Rechargeable professional automated external defibrillator
Philips System Case, Rigid, FR3
PHILIPS ELECTRONICS NORTH AMERICA CORPORATION
FR3 System Case, Ridge
In Commercial Distribution

  • 00884838055704 ()
989803149971

  • Rechargeable professional automated external defibrillator
Cannula, Case of 25, Nasal
Ambu A/S
814300-000/25
In Commercial Distribution

  • 05707480041794 ()
  • 05707480133925 ()

  • Adult
814300-000/25

  • Polysomnograph
Perfit Ace Adjustable 30/case
Ambu A/S
000281000
In Commercial Distribution

  • 05707480018420 ()
  • 05707480024636 ()

  • Adult
000281000

  • Cervical spine collar, single-use
CASE 905-890 PYRAMESH SHORT IMPLANT
MEDTRONIC SOFAMOR DANEK, INC.
905-890
In Commercial Distribution

  • 00673978081243 ()


  • Instrument tray, reusable
CASE 900-916 POSTERIOR 16MM INNER
MEDTRONIC SOFAMOR DANEK, INC.
900-916
In Commercial Distribution

  • 00673978957043 ()


  • Instrument tray, reusable
CASE 900-914 POSTERIOR 14MM INNER
MEDTRONIC SOFAMOR DANEK, INC.
900-914
In Commercial Distribution

  • 00673978957036 ()


  • Instrument tray, reusable
CASE 185.049 M8 IMPLANT LID
MEDTRONIC SOFAMOR DANEK, INC.
185.049
In Commercial Distribution

  • 00673978944760 ()


  • Instrument tray, reusable
CASE 950-900B TRAY ENDO-CURRETTE 5.10MM
MEDTRONIC SOFAMOR DANEK, INC.
950-900B
In Commercial Distribution

  • 00673978083803 ()


  • Instrument tray, reusable
CASE 905-891 PYRAMESH TALL IMPLANT
MEDTRONIC SOFAMOR DANEK, INC.
905-891
In Commercial Distribution

  • 00673978081250 ()


  • Instrument tray, reusable
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