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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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1-piece, monofocal, hydrophobic, acrylic, intraocular lens, +16.0D
CARL ZEISS MEDITEC PRODUCTION, LLC
CT LUCIA 611P.AM DPT 16.0
In Commercial Distribution

  • 00843045103509 ()
003500-0056-654

  • Posterior-chamber intraocular lens, pseudophakic
1-piece, monofocal, hydrophobic, acrylic, intraocular lens, +15.5D
CARL ZEISS MEDITEC PRODUCTION, LLC
CT LUCIA 611P.AM DPT 15.5
In Commercial Distribution

  • 00843045103493 ()
003500-0056-653

  • Posterior-chamber intraocular lens, pseudophakic
1-piece, monofocal, hydrophobic, acrylic, intraocular lens, +15.0D
CARL ZEISS MEDITEC PRODUCTION, LLC
CT LUCIA 611P.AM DPT 15.0
In Commercial Distribution

  • 00843045103486 ()
003500-0056-652

  • Posterior-chamber intraocular lens, pseudophakic
1-piece, monofocal, hydrophobic, acrylic, intraocular lens, +14.5D
CARL ZEISS MEDITEC PRODUCTION, LLC
CT LUCIA 611P.AM DPT 14.5
In Commercial Distribution

  • 00843045103479 ()
003500-0056-651

  • Posterior-chamber intraocular lens, pseudophakic
1-piece, monofocal, hydrophobic, acrylic, intraocular lens, +14.0D
CARL ZEISS MEDITEC PRODUCTION, LLC
CT LUCIA 611P.AM DPT 14.0
In Commercial Distribution

  • 00843045103462 ()
003500-0056-650

  • Posterior-chamber intraocular lens, pseudophakic
1-piece, monofocal, hydrophobic, acrylic, intraocular lens, +13.5D
CARL ZEISS MEDITEC PRODUCTION, LLC
CT LUCIA 611P.AM DPT 13.5
In Commercial Distribution

  • 00843045103455 ()
003500-0056-649

  • Posterior-chamber intraocular lens, pseudophakic
No Description
COCHLEAR LIMITED
Z145225
In Commercial Distribution

  • 09321502014557 ()
Z145225

  • ENT surgical procedure kit, non-medicated, reusable
instrument loaner set
Paradigm Spine GmbH
UQS00100
In Commercial Distribution

  • 04260636678998 ()
UQS00100

  • General internal orthopaedic fixation system implantation kit
The Occlutech Atrial Septal Defect (ASD) Occluder is a percutaneous transcatheter closure device, consisting of 2 nitinol wire mesh discs connected by a waist section and polyethylene terephthalate (PET) patches. The PET patches, sewn into the wire mesh, are intended to stop the blood flow through the ASD as well as optimize tissue growth. The design properties of the Occlutech ASD Occluder allow transcatheter implant of the device. The Occlutech ASD Occluder is packaged with its compatible Occlutech Pistol Pusher (OPP), Instructions for Use (IFU) and Patient Implant Card.
Occlutech GmbH
37ASD33
In Commercial Distribution

  • 04260182521687 ()

  • Outer Diameter: 33 Millimeter
37ASD33

  • Cardiac defect occluder
The Occlutech Atrial Septal Defect (ASD) Occluder is a percutaneous transcatheter closure device, consisting of 2 nitinol wire mesh discs connected by a waist section and polyethylene terephthalate (PET) patches. The PET patches, sewn into the wire mesh, are intended to stop the blood flow through the ASD as well as optimize tissue growth. The design properties of the Occlutech ASD Occluder allow transcatheter implant of the device. The Occlutech ASD Occluder is packaged with its compatible Occlutech Pistol Pusher (OPP), Instructions for Use (IFU) and Patient Implant Card.
Occlutech GmbH
37ASD30
In Commercial Distribution

  • 04260182521670 ()

  • Outer Diameter: 30 Millimeter
37ASD30

  • Cardiac defect occluder
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