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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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BF BIPAL 7F 50CM 2.2MM JAW
CORDIS CORPORATION
502402B
In Commercial Distribution

  • 20705032054956 ()
502402B

  • Endomyocardial biopsy forceps, single-use
BF BIPAL 7F 50CM 2.2MM MP-TIP
CORDIS CORPORATION
502402M
In Commercial Distribution

  • 20705032054963 ()
502402M

  • Endomyocardial biopsy forceps, single-use
BF BIPAL 7F 104CM 2.2MM JAW
CORDIS CORPORATION
502400B
In Commercial Distribution

  • 20705032054949 ()
502400B

  • Endomyocardial biopsy forceps, single-use
Micro Elevator
Stryker GmbH
4035
In Commercial Distribution

  • 07613327363159 ()
4035

  • Bone lever/elevator, reusable
No Description
MEDITECH SPINE, LLC
613-271719-15
In Commercial Distribution

  • B167613271719150 ()


  • Surgical implant/trial-implant/sizer holder, reusable
No Description
MEDITECH SPINE, LLC
613-271719-07
In Commercial Distribution

  • B167613271719070 ()


  • Surgical implant/trial-implant/sizer holder, reusable
No Description
MEDITECH SPINE, LLC
613-271719-00
In Commercial Distribution

  • B167613271719000 ()


  • Surgical implant/trial-implant/sizer holder, reusable
No Description
MEDITECH SPINE, LLC
613-271718-15
In Commercial Distribution

  • B167613271718150 ()


  • Surgical implant/trial-implant/sizer holder, reusable
No Description
MEDITECH SPINE, LLC
613-271718-07
In Commercial Distribution

  • B167613271718070 ()


  • Surgical implant/trial-implant/sizer holder, reusable
No Description
MEDITECH SPINE, LLC
613-271718-00
In Commercial Distribution

  • B167613271718000 ()


  • Surgical implant/trial-implant/sizer holder, reusable
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