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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Softshell Venous Reser. 800ml, Blood Transfer Bag 1000 ml - 2 spike ports, Gas Filter
DATASCOPE CORP.
BO-T 51502
Not in Commercial Distribution

  • 00607567211346 ()
709000385

  • Cardiopulmonary bypass system blood tubing set
No Description
DATASCOPE CORP.
BO-T 4930
Not in Commercial Distribution

  • 00607567211278 ()
709000383

  • Cardiopulmonary bypass system blood tubing set
No Description
DATASCOPE CORP.
BO-T 37309
Not in Commercial Distribution

  • 00607567211049 ()
701068727

  • Cardiopulmonary bypass system blood tubing set
No Description
DATASCOPE CORP.
BO-T 37307
Not in Commercial Distribution

  • 00607567211032 ()
701068723

  • Cardiopulmonary bypass system blood tubing set
No Description
DATASCOPE CORP.
BO-T 55004
Not in Commercial Distribution

  • 00607567211025 ()
709000276

  • Cardiopulmonary bypass system blood tubing set
No Description
DATASCOPE CORP.
BO-T 55003
Not in Commercial Distribution

  • 00607567211018 ()
709000274

  • Cardiopulmonary bypass system blood tubing set
No Description
DATASCOPE CORP.
BO-T 55002
Not in Commercial Distribution

  • 00607567211001 ()
709000272

  • Cardiopulmonary bypass system blood tubing set
No Description
DATASCOPE CORP.
BO-T 55001
Not in Commercial Distribution

  • 00607567210998 ()
709000270

  • Cardiopulmonary bypass system blood tubing set
No Description
DATASCOPE CORP.
BO-T 55000
Not in Commercial Distribution

  • 00607567210981 ()
709000268

  • Cardiopulmonary bypass system blood tubing set
BO-RF32 RotaFlow,
DATASCOPE CORP.
BO-T 8040
Not in Commercial Distribution

  • 00607567210165 ()
709000323

  • Cardiopulmonary bypass system blood tubing set
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