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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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TRIAL REFLECTION LINER XLPE 40 ID 20 DEG ANT +4 58-60 G
Smith & Nephew, Inc.
71934296
In Commercial Distribution

  • 00885556143070 ()
71934296

  • General internal orthopaedic fixation system implantation kit
TRIAL REFLECTION LINER XLPE 40 ID 20 DEG ANT +4 62-64 H
Smith & Nephew, Inc.
71934297
In Commercial Distribution

  • 00885556143063 ()
71934297

  • General internal orthopaedic fixation system implantation kit
21GA (0.85MM OD;0.60MM ID) X 7CM SAFETY NEEDLE W/ECHO TIP
Medical Components, Inc.
DMC217S
In Commercial Distribution

  • 50884908143657 ()
  • 00884908143652 ()


  • Vascular catheter introduction needle
21GA (0.85MM OD;0.60MM ID) X 5CM SAFETY NEEDLE W/ECHO TIP
Medical Components, Inc.
DMC215S
In Commercial Distribution

  • 50884908143626 ()
  • 00884908143621 ()


  • Vascular catheter introduction needle
ESOPHAGOSCOPE-TUBE ID 4.4MM OD 5.7mm, TL 200mm, with proximal light connection, reusable
Richard Wolf GmbH
827040
Not in Commercial Distribution

  • 04055207009536 ()

  • Lumen/Inner Diameter: 4.4 Millimeter
8270.40

  • Rigid optical oesophagoscope
The scanner can be used to quickly enter the user ID, the ID on a basket’s anti-reflection tag, or the lot or batch number of a reagent.
LEICA BIOSYSTEMS MELBOURNE PTY LTD
HistoCore PELORIS 3 Barcode Scanner Kit
In Commercial Distribution

  • 09349458005566 ()
S45.4508

  • Tissue processor IVD, automated/semi-automated
Control Swabs intended for use only with the ID NOW™ COVID-19 2.0 product. Refer to the ID NOW COVID-19 2.0 Product Insert for instructions for use.
Alere Scarborough, Inc.
192-080
In Commercial Distribution

  • 00811877011361 ()


  • SARS-CoV-2 nucleic acid IVD, control
PLATE DRY CLI GRAM+ ID AUTO -A semi-quantitative test intended for the automated identification of Gram negative bacterial isolates based on biochemical reactions. Used in a diagnostic workflow to aid clinicians in determining potential treatment options for patients suspected of having a microbial infection, the device requires an automated system to produce a result and requires a pure, agar grown culture. This device is for professional use only and is not a companion diagnostic.
REMEL, INC.
GNID
In Commercial Distribution

  • 00848838074325 ()


  • Multiple aerobic gram positive bacteria species culture isolate identification IVD, kit
Clean-Bor Tube
Vacumed
1013-60-BULK
In Commercial Distribution

  • 00850644007916 ()
  • 08506440079160 ()
1013-60-BULK

  • Gas-sampling/monitoring respiratory tubing, single-use
Clean-Bor Tube
Vacumed
1013-60
In Commercial Distribution

  • 00850644007909 ()
1013-60

  • Gas-sampling/monitoring respiratory tubing, single-use
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