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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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WoundSeal® Rapid Response
BIOLIFE, L.L.C.
WSO001Z
In Commercial Distribution

  • 00834061003201 ()
  • 00834061006400 ()
WSO001Z

  • Non-organic haemostatic agent
WoundSeal® Rapid Response
BIOLIFE, L.L.C.
WSO001GC
In Commercial Distribution

  • 00834061003195 ()
  • 00834061006394 ()
WSO001GC

  • Non-organic haemostatic agent
WoundSeal® Powder
BIOLIFE, L.L.C.
WSO310
In Commercial Distribution

  • 00834061003102 ()
  • 00834061003515 ()
  • 00834061000279 ()
WSO310

  • Non-organic haemostatic agent
WoundSeal® Powder
BIOLIFE, L.L.C.
WSO310C
In Commercial Distribution

  • 00834061000491 ()
  • 00834061001399 ()
  • 00834061000279 ()
WSO310C

  • Non-organic haemostatic agent
WoundSeal® Powder
BIOLIFE, L.L.C.
WSO310ZC
In Commercial Distribution

  • 00834061000477 ()
  • 00834061001412 ()
  • 00834061000279 ()
WSO310ZC

  • Non-organic haemostatic agent
WoundSeal® Powder
BIOLIFE, L.L.C.
WSO310GC
In Commercial Distribution

  • 00834061000453 ()
  • 00834061001405 ()
  • 00834061000279 ()
WSO310GC

  • Non-organic haemostatic agent
WoundSeal® + Applicator
BIOLIFE, L.L.C.
QSO010ZC
In Commercial Distribution

  • 00834061000446 ()
  • 00834061000118 ()
  • 00834061000286 ()
QSO010ZC

  • Non-organic haemostatic agent
WoundSeal® + Applicator
BIOLIFE, L.L.C.
QSO010GC
In Commercial Distribution

  • 00834061000392 ()
  • 00834061001382 ()
  • 00834061000286 ()
QSO010GC

  • Non-organic haemostatic agent
WoundSeal® + Applicator
BIOLIFE, L.L.C.
QSO020C
In Commercial Distribution

  • 00834061000378 ()
  • 00834061001375 ()
QSO020C

  • Non-organic haemostatic agent
WoundSeal® Powder
BIOLIFE, L.L.C.
WSO1001C
In Commercial Distribution

  • 00834061002358 ()
  • 00834061000354 ()
WSO1001C

  • Non-organic haemostatic agent
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