SEARCH RESULTS FOR: ("St. Joseph")(21058 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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DK Lube Jelly 4oz tube, ST
Dukal LLC
880
In Commercial Distribution

  • 20665973010193 ()
  • 10665973010196 ()
  • 00665973010199 ()
880

  • General-body orifice lubricant
DK Lube Jelly 2oz tube, ST
Dukal LLC
879
In Commercial Distribution

  • 10665973010189 ()
  • 00665973010182 ()
  • 20665973010186 ()
879

  • General-body orifice lubricant
DK Lube Jelly 5gm Pack, ST
Dukal LLC
878
In Commercial Distribution

  • 10665973010172 ()
  • 00665973010175 ()
  • 20665973010179 ()
878

  • General-body orifice lubricant
DK Lube Jelly 3gm pack, ST
Dukal LLC
877
In Commercial Distribution

  • 20665973010162 ()
  • 10665973010165 ()
  • 00665973010168 ()
877

  • General-body orifice lubricant
DK Fen Surg Drape 18x26, ST
Dukal LLC
20-001
In Commercial Distribution

  • 20665973006738 ()
  • 10665973006731 ()
  • 00665973006734 ()
20-001

  • Patient surgical drape, single-use
REPL FSP SFT 14FR 14 ST
REPRO MED SYSTEMS, INC.
R1F1S1L4S
In Commercial Distribution

  • 00659443002623 ()
R1F1S1L4S

  • Emergency airway clearance suction system, manual
REPL FSP RGD 14FR 14 ST
REPRO MED SYSTEMS, INC.
R1F1R1L4S
In Commercial Distribution

  • 00659443002548 ()
R1F1R1L4S

  • Emergency airway clearance suction system, manual
REPL FSP 2-14FR 14 Cath ST
REPRO MED SYSTEMS, INC.
R1F002L4S
In Commercial Distribution

  • 00659443002388 ()
R1F002L4S

  • Emergency airway clearance suction system, manual
REPL FSP 14FR 35/14 ST
REPRO MED SYSTEMS, INC.
R1F00114S
In Commercial Distribution

  • 00659443002333 ()
R1F00114S

  • Emergency airway clearance suction system, manual
REPL FSP 10FR 35/14 ST
REPRO MED SYSTEMS, INC.
R1F00110S
In Commercial Distribution

  • 00659443002326 ()
R1F00110S

  • Emergency airway clearance suction system, manual
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