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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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Overall size 24”W x 20.5”D x 24.5”T. 3.0 Cubic ft. storage Chamber I.D. 20”W x 17"D x 15.25”T Temperature Range: 90-160 F Accuracy +/- 1 degrees F Digital control Glass door Audible and visual over-temp alarm Keyed temperature lock for each chamber Data Logger Door Lock Foot levelers Electrical: 120V, 3.5 Amp, 50/60 Hz. .45kw/hr, 1537 btu/hr. UL/CUL listed FDA Registered
M.A.C. MEDICAL INC.
SWC182424-G-NB
In Commercial Distribution

  • B286SWC182424GNB1 ()
SWC182424-G-NB

  • Blanket warming cabinet, dry-heat
Overall size 24”W x 20.5”D x 24.5”T. 3.0 Cubic ft. storage Chamber I.D. 20”W x 17"D x 15.25”T Temperature Range: 90-160 F Accuracy +/- 1 degrees F Digital control. Glass door Data logger Door lock Audible and visual over-temp alarm. Keyed temperature lock for each chamber Mobile Base Electrical: 120V, 3.5 Amp, 50/60 Hz. .45kw/hr, 1537 btu/hr. UL/CUL listed FDA Registered
M.A.C. MEDICAL INC.
SWC182424-G-MB
In Commercial Distribution

  • B286SWC182424GMB1 ()
SWC182424-G-MB

  • Blanket warming cabinet, dry-heat
Overall size 24”W x 20.5”D x 24.5”T. 3.0 Cubic ft. storage Chamber I.D. 20”W x 17"D x 15.25”T Temperature Range: 90-160 F Accuracy +/- 1 degrees F Digital control. Glass door Data logger Door lock Audible and visual over-temp alarm. Keyed temperature lock for each chamber 4" Base Electrical: 120V, 3.5 Amp, 50/60 Hz. .45kw/hr, 1537 btu/hr. UL/CUL listed FDA Registered
M.A.C. MEDICAL INC.
SWC182424-G-4B
In Commercial Distribution

  • B286SWC182424G4B1 ()
SWC182424-G-4B

  • Blanket warming cabinet, dry-heat
Overall size 24”W x 20.5”D x 24.5”T. 3.0 Cubic ft. storage Chamber I.D. 20”W x 17"D x 15.25”T Temperature Range: 90-160 F Accuracy +/- 1 degrees F Digital control. Stainless Steel door Data logger Door lock Audible and visual over-temp alarm. Keyed temperature lock for each chamber 4" Base Electrical: 120V, 3.5 Amp, 50/60 Hz. .45kw/hr, 1537 btu/hr. UL/CUL listed FDA Registered
M.A.C. MEDICAL INC.
SWC182424-4B
In Commercial Distribution

  • B286SWC1824244B1 ()
SWC182424-4B

  • Blanket warming cabinet, dry-heat
Size: 18 mm
Boston Medical Products, Inc.
450018
Not in Commercial Distribution

  • EBES4500180 ()
  • EBES4500181 ()

  • Length (Outer Limb): 76 mm
  • Outer Diameter (Outer Limb): 14 mm
  • Length (Lower Inner Limb): 39 mm
  • Length (Upper Inner Limb): 24 mm
  • Length (Inner Limb): 77 mm
  • Outer Diameter (Inner Limb): 18 mm
450018

  • Trachea prosthesis
Size: Standard 13 mm; Type: Radiopaque
Boston Medical Products, Inc.
42013R
In Commercial Distribution

  • EBES42013R0 ()
  • EBES42013R1 ()

  • Length (Outer Limb): 55 mm
  • Outer Diameter (Outer Limb): 11 mm
  • Length (Lower Inner Limb): 34 mm
  • Length (Upper Inner Limb): 24 mm
  • Length (Inner Limb): 69 mm
  • Outer Diameter (Inner Limb): 13 mm
42013R

  • Trachea prosthesis
Size: Standard 13 mm; Type: Clear
Boston Medical Products, Inc.
420013
In Commercial Distribution

  • EBES4200130 ()
  • EBES4200131 ()

  • Length (Outer Limb): 55 mm
  • Outer Diameter (Outer Limb): 11 mm
  • Length (Lower Inner Limb): 34 mm
  • Length (Upper Inner Limb): 24 mm
  • Length (Inner Limb): 69 mm
  • Outer Diameter (Inner Limb): 13 mm
420013

  • Trachea prosthesis
The aiACT Kit is an in vitro diagnostic test for use with the Sonoclot® Coagulation & Platelet Function Analyzer System. The aiACT test is an activated whole blood clotting time test which uses a blend of celite and clay for contact activation. It may also be used with citrated whole blood. The aiACT Kit is only intended for high dose (ACT greater or equal to 400 seconds, on Sonoclot Analyzer) heparin anticoagulation management as typically encountered during cardiopulmonary bypass surgery. The aiACT test provides ACT results that are substantially unaffected by aprotinin. When used with the Sonoclot Analyzer System, the aiACT test provides quantitative Onset/ACT and Clot Rate results. Do not use the aiACT test for platelet function assessment. Each kit contains 24 lidded yellow plastic activation cuvettes, 24 probes, and instructions for use. The activation cuvettes contain a controlled amount of contact activator and a magnetic stir bar.
SIENCO, INC.
800-0441
In Commercial Distribution

  • B55880004410 ()
  • B55880004411 ()
800-0441

  • Multiple coagulation factor IVD, kit, clotting
Aquasil Ultra DenPlant™ Smart Wetting® Impression Material Introductory Kit
DENTSPLY INTERNATIONAL INC.
678169
Not in Commercial Distribution

  • D0026781691 ()

  • Total Volume: 50 Milliliter
  • 1 Cartridge Monophase RS, 2 Cartridges LV RS, 3 Cartridges XLV RS, 2 Cartridges Rigid FS, 24 Mixing Tips, 12 Intraoral Tips, 1 Bottle Adhesive, 1 Strong Massad DenPlant™ Tray Kit (12 trays total)
678169

  • Silicone dental impression material
Overall size 24”W x 20.5”D x 24.5”T. 3.0 Cubic ft. storage Chamber I.D. 20”W x 17"D x 15.25”T Temperature Range: 90-160 F Accuracy +/- 1 degrees F Digital control. Glass door Audible and visual over-temp alarm. Keyed temperature lock for each chamber Electronic Locking door Data Logger Foot levelers No base Electrical: 120V, 3.5 Amp, 50/60 Hz. .45kw/hr, 1537 btu/hr. UL/CUL listed FDA Registered
M.A.C. MEDICAL INC.
W2024XSS-G-NB-BWEL
In Commercial Distribution

  • B286W2024XSSGNBBWEL1 ()
W2024XSS-G-NB-BWEL

  • Blanket warming cabinet, dry-heat
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