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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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Automated External Defibrillator
HEARTSINE TECHNOLOGIES LTD
SAM360P
In Commercial Distribution

  • 05060167120718 ()
360-STR-US-AV

  • Non-rechargeable public automated external defibrillator
Automated External Defibrillator
HEARTSINE TECHNOLOGIES LTD
SAM450P
In Commercial Distribution

  • 05060167120695 ()
450-STR-US-10

  • Non-rechargeable public semi-automated external defibrillator
Automated External Defibrillator
HEARTSINE TECHNOLOGIES LTD
SAM 360P
In Commercial Distribution

  • 05060167120688 ()
360-STR-US-10

  • Non-rechargeable public automated external defibrillator
i-FACTOR™ Putty, 5.0 cc Syringe
Cerapedics Inc.
700-050
In Commercial Distribution

700-050

  • Bone matrix implant, animal-derived, bioabsorbable
i-FACTOR Putty, 2.5cc Syringe
Cerapedics Inc.
700-025
In Commercial Distribution

700-025

  • Bone matrix implant, animal-derived, bioabsorbable
i-FACTOR Putty, 1.0cc Syringe
Cerapedics Inc.
700-010
In Commercial Distribution

700-010

  • Bone matrix implant, animal-derived, bioabsorbable
MON 24950L USA MKT M10.2 USA MKT
MEDTRONIC, INC.
24950L
In Commercial Distribution

  • 00643169552272 ()


  • Cardiac pulse generator reader, home-use
MON 24950L USA MKT M10.2 USA
MEDTRONIC, INC.
24950L
In Commercial Distribution

  • 00643169552043 ()


  • Cardiac pulse generator reader, home-use
Clareon PanOptix UVA
Alcon Laboratories, Inc.
CCWTT0
In Commercial Distribution

  • 00380652413794 ()


  • Posterior-chamber intraocular lens, pseudophakic
Clareon PanOptix UVA
Alcon Laboratories, Inc.
CCWTT0
In Commercial Distribution

  • 00380652413787 ()


  • Posterior-chamber intraocular lens, pseudophakic
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