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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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No Description
FGX INTERNATIONAL INC.
10248850.FTG
In Commercial Distribution

  • 00193033076323 ()


  • Tinted non-prescription spectacles
No Description
FGX INTERNATIONAL INC.
10248848.FTG
In Commercial Distribution

  • 00193033076316 ()


  • Tinted non-prescription spectacles
No Description
FGX INTERNATIONAL INC.
10248855.FTG
In Commercial Distribution

  • 00193033076194 ()


  • Tinted non-prescription spectacles
No Description
FGX INTERNATIONAL INC.
10248847.FTG
In Commercial Distribution

  • 00193033076170 ()


  • Tinted non-prescription spectacles
No Description
FGX INTERNATIONAL INC.
10248854.FTG
In Commercial Distribution

  • 00193033076774 ()


  • Tinted non-prescription spectacles
No Description
FGX INTERNATIONAL INC.
10248852.FTG
In Commercial Distribution

  • 00193033076767 ()


  • Tinted non-prescription spectacles
No Description
FGX INTERNATIONAL INC.
10248011.FWM
In Commercial Distribution

  • 00193033057131 ()


  • Tinted non-prescription spectacles
No Description
FGX INTERNATIONAL INC.
10248005.FWM
In Commercial Distribution

  • 00193033057070 ()


  • Tinted non-prescription spectacles
Prospera Transparent Film Dressing
DEROYAL INDUSTRIES, INC.
MR304-0447
In Commercial Distribution

  • 50749756668700 ()
  • 00749756668705 ()
MR304-0447

  • Synthetic polymer semi-permeable film dressing, adhesive
Prospera Transparent Film Dressing
DEROYAL INDUSTRIES, INC.
MR303-0812
In Commercial Distribution

  • 50749756657360 ()
  • 00749756657365 ()
MR303-0812

  • Synthetic polymer semi-permeable film dressing, adhesive
No Description
FGX INTERNATIONAL INC.
10236768.FTG
In Commercial Distribution

  • 00887661273758 ()


  • Tinted non-prescription spectacles
No Description
FGX INTERNATIONAL INC.
10236764.FTG
In Commercial Distribution

  • 00887661273734 ()


  • Tinted non-prescription spectacles
No Description
FGX INTERNATIONAL INC.
10236757.FTG
In Commercial Distribution

  • 00887661273543 ()


  • Tinted non-prescription spectacles
No Description
FGX INTERNATIONAL INC.
10238895.FTG
In Commercial Distribution

  • 00887661453235 ()


  • Tinted non-prescription spectacles
No Description
FGX INTERNATIONAL INC.
ASTSNR-9&CO.LTS
In Commercial Distribution

  • 00887661784391 ()


  • Tinted non-prescription spectacles
No Description
FGX INTERNATIONAL INC.
10242794.FTG
In Commercial Distribution

  • 00887661544810 ()


  • Tinted non-prescription spectacles
No Description
FGX INTERNATIONAL INC.
10242814.FTG
In Commercial Distribution

  • 00887661545039 ()


  • Tinted non-prescription spectacles
No Description
FGX INTERNATIONAL INC.
10242813.FTG
In Commercial Distribution

  • 00887661545022 ()


  • Tinted non-prescription spectacles
No Description
FGX INTERNATIONAL INC.
10242809.FTG
In Commercial Distribution

  • 00887661544988 ()


  • Tinted non-prescription spectacles
No Description
FGX INTERNATIONAL INC.
10242807.FTG
In Commercial Distribution

  • 00887661544964 ()


  • Tinted non-prescription spectacles
No Description
FGX INTERNATIONAL INC.
10242805.FTG
In Commercial Distribution

  • 00887661544933 ()


  • Tinted non-prescription spectacles
No Description
FGX INTERNATIONAL INC.
10242803.FTG
In Commercial Distribution

  • 00887661544919 ()


  • Tinted non-prescription spectacles
No Description
FGX INTERNATIONAL INC.
10242801.FTG
In Commercial Distribution

  • 00887661544896 ()


  • Tinted non-prescription spectacles
No Description
FGX INTERNATIONAL INC.
10242800.FTG
In Commercial Distribution

  • 00887661544889 ()


  • Tinted non-prescription spectacles
No Description
FGX INTERNATIONAL INC.
10242799.FTG
In Commercial Distribution

  • 00887661544872 ()


  • Tinted non-prescription spectacles
No Description
FGX INTERNATIONAL INC.
10242798.FTG
In Commercial Distribution

  • 00887661544865 ()


  • Tinted non-prescription spectacles
No Description
FGX INTERNATIONAL INC.
10242795.FTG
In Commercial Distribution

  • 00887661544834 ()


  • Tinted non-prescription spectacles
FIZE kUO Disposable Kit catalog number for 1 pc: FI-KT00-KU01-0007 FIZE kUO Disposable Kit catalog number for 10 pcs: FI-FG00-KU03-0003
FIZE RESEARCH LTD
G2
In Commercial Distribution

  • 17290019239212 ()
  • 07290019239215 ()
FI-KT00-KU01-0007

  • Urine monitoring system
HOMECARE BARIATRIC BED, HEIGHT 18.5"-26", DIMENSIONS: 48"(W) x 88"(L), WT LIMIT 750 lbs. (WEIGHT LIMIT INCLUDES PATIENT WEIGHT, MATTRESS WEIGHT, RAILS AND ANY ACCESSORIES)
DALTON MEDICAL CORPORATION
B-T5048
In Commercial Distribution

  • 00815027011508 ()

  • DIMENSIONS: 48" W x 88' L


  • Basic electric home bed
No Description
BIOMET SPINE LLC
14-522488E
In Commercial Distribution

  • 00880304983908 ()

  • 4 Level 88 mm Fixed Plate
14-522488E

  • Bone-screw internal spinal fixation system, sterile
No Description
Biomet Orthopedics, LLC
105427
In Commercial Distribution

  • 00880304191686 ()

  • 27 SIZE
105427

  • Acetabular shell
No Description
Biomet Orthopedics, LLC
106027
In Commercial Distribution

  • 00880304455061 ()

  • 27 SIZE
106027

  • Acetabular shell
No Description
Biomet Orthopedics, LLC
11-302127
In Commercial Distribution

  • 00880304493964 ()

  • 27 MM
11-302127

  • Uncoated hip femur prosthesis, modular
No Description
Biomet Orthopedics, LLC
110005136
In Commercial Distribution

  • 00880304567849 ()

  • SIZE 27
110005136

  • Orthopaedic implant impactor, reusable
No Description
Biomet Orthopedics, LLC
110005131
In Commercial Distribution

  • 00880304567795 ()

  • SIZE 27
110005131

  • Orthopaedic implant impactor, reusable
No Description
Biomet Orthopedics, LLC
178569
In Commercial Distribution

  • 00880304554825 ()

  • 27 MM
178569

  • Knee femur stem prosthesis
No Description
Biomet Uk Ltd
31-400627
In Commercial Distribution

  • 05019279415359 ()

  • SIZE 27
31-400627

  • Orthopaedic implant impactor, reusable
S2S CrossBar, 27 - 35mm. The Sierra occipito-cervico-thoracic (OCT) spinal fixation system, including polyaxial screws, rods, locking caps, occipital plates, occipital screws, lateral connectors, contoured crossbars, hooks, and components, is used to provide stabilization of the spine in order to permit the biological process of spinal fusion to occur. Accepted standard techniques of spinal fusion are an integral part of the implantation of this system.
Seaspine Orthopedics Corporation
50-2022
Not in Commercial Distribution

  • 10889910059158 ()

  • 27 - 35mm
50-2022

  • Vertebral body prosthesis, non-sterile
AcrySof(R) IQ TORIC ASTIGMATISM IOL, SINGLE-PIECE ACRYLIC FOLDABLE LENS, UV WITH BLUE LIGHTFILTER, 13.0mm LENGTH, 6.0mm BICONVEX TORICASPHERIC OPTIC, 1.50 D CYLINDER.
Alcon Laboratories, Inc.
SN6AT3
In Commercial Distribution

  • 00380652250030 ()

  • Diopter 27
SN6AT3.270

  • Posterior-chamber intraocular lens, pseudophakic
AcrySof(R) IQ ASPHERIC IOL, SP ACRYLIC FOLDABLELENS, w/AcrySert(R) DELIVERY SYSTEM, UV w/BLUELIGHT FILTER, 13.0mm LENGTH, 6.0mm ANTERIORASYMMETRIC BICONVEX OPTIC, PLANAR HAPTICS.
Alcon Laboratories, Inc.
SN6CWS
Not in Commercial Distribution

  • 00380652249355 ()

  • Diopter 27
SN6CWS.270

  • Posterior-chamber intraocular lens, pseudophakic
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