SEARCH RESULTS FOR: (*Make St. Paul*)(3394 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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PUMP 2FSP RGD/SFT ALL CATHETER ST
REPRO MED SYSTEMS, INC.
P2F1B1AFS
In Commercial Distribution

  • 00659443002210 ()
P2F1B1AFS

  • Emergency airway clearance suction system, manual
PUMP 2FSP 8/10FR 35/14 ST
REPRO MED SYSTEMS, INC.
P2F00181S
In Commercial Distribution

  • 00659443002180 ()
P2F00181S

  • Emergency airway clearance suction system, manual
PUMP NSC SOFT 14FR 35/14 ST
REPRO MED SYSTEMS, INC.
P1N1S114S
In Commercial Distribution

  • 00659443002142 ()
P1N1S114S

  • Emergency airway clearance suction system, manual
PUMP NSC SOFT 10FR 35/14 ST
REPRO MED SYSTEMS, INC.
P1N1S110S
In Commercial Distribution

  • 00659443002128 ()
P1N1S110S

  • Emergency airway clearance suction system, manual
PUMP NSC RIGID 10FR 35/14 ST
REPRO MED SYSTEMS, INC.
P1N1R110S
In Commercial Distribution

  • 00659443002043 ()
P1N1R110S

  • Emergency airway clearance suction system, manual
PUMP NSC 8FR 10FR 35/14 ST
REPRO MED SYSTEMS, INC.
P1N00181S
In Commercial Distribution

  • 00659443001961 ()
P1N00181S

  • Emergency airway clearance suction system, manual
PUMP FSP S0FT 14FR 35/14 ST
REPRO MED SYSTEMS, INC.
P1F1S114S
In Commercial Distribution

  • 00659443001794 ()
P1F1S114S

  • Emergency airway clearance suction system, manual
PUMP FSP RIGID W/ET ADPT ST
REPRO MED SYSTEMS, INC.
P1F1E000S
In Commercial Distribution

  • 00659443001572 ()
P1F1E000S

  • Emergency airway clearance suction system, manual
PUMP FSP R/S ALL CATHETER ST
REPRO MED SYSTEMS, INC.
P1F1B1AFS
In Commercial Distribution

  • 00659443001558 ()
P1F1B1AFS

  • Emergency airway clearance suction system, manual
PUMP FSP 8/10FR 35/14 ST
REPRO MED SYSTEMS, INC.
P1F00181S
In Commercial Distribution

  • 00659443001411 ()
P1F00181S

  • Emergency airway clearance suction system, manual
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