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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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Consensus® Hip System - 00844588000539

Acetabular Insert, 20° Hood
CONSENSUS ORTHOPEDICS, INC.
1004-0-3264
Not in Commercial Distribution

  • 00844588000539 ()

  • Outer Diameter: 32 Millimeter
1004-0-3264

  • Non-constrained polyethylene acetabular liner

Consensus® Hip System - 00844588000522

Acetabular Insert, 20° Hood
CONSENSUS ORTHOPEDICS, INC.
1004-0-3262
Not in Commercial Distribution

  • 00844588000522 ()

  • Outer Diameter: 32 Millimeter
1004-0-3262

  • Non-constrained polyethylene acetabular liner

Consensus® Hip System - 00844588000515

Acetabular Insert, 20° Hood
CONSENSUS ORTHOPEDICS, INC.
1004-0-3260
Not in Commercial Distribution

  • 00844588000515 ()

  • Outer Diameter: 32 Millimeter
1004-0-3260

  • Non-constrained polyethylene acetabular liner

Consensus® Hip System - 00844588000508

Acetabular Insert, 20° Hood
CONSENSUS ORTHOPEDICS, INC.
1004-0-3258
Not in Commercial Distribution

  • 00844588000508 ()

  • Outer Diameter: 32 Millimeter
1004-0-3258

  • Non-constrained polyethylene acetabular liner

Consensus® Hip System - 00844588000492

Acetabular Insert, 20° Hood
CONSENSUS ORTHOPEDICS, INC.
1004-0-3256
Not in Commercial Distribution

  • 00844588000492 ()

  • Outer Diameter: 32 Millimeter
1004-0-3256

  • Non-constrained polyethylene acetabular liner

Consensus® Hip System - 00844588000485

Acetabular Insert, 20° Hood
CONSENSUS ORTHOPEDICS, INC.
1004-0-3254
Not in Commercial Distribution

  • 00844588000485 ()

  • Outer Diameter: 32 Millimeter
1004-0-3254

  • Non-constrained polyethylene acetabular liner

Consensus® Hip System - 00844588000478

Acetabular Insert, 20° Hood
CONSENSUS ORTHOPEDICS, INC.
1004-0-3252
Not in Commercial Distribution

  • 00844588000478 ()

  • Outer Diameter: 32 Millimeter
1004-0-3252

  • Non-constrained polyethylene acetabular liner

Ambu® SPUR® II Pediatric Resuscitator - 05707480149971

w/PEEP Valve 20
Ambu A/S
530215001
In Commercial Distribution

  • 05707480149988 ()
  • 05707480149971 ()
530215001

  • Pulmonary resuscitator, manual, single-use

Ambu® SPUR® II Adult Resuscitator - 05707480149711

w/PEEP Valve 20
Ambu A/S
524611011
In Commercial Distribution

  • 05707480149728 ()
  • 05707480149711 ()
524611011

  • Pulmonary resuscitator, manual, single-use

NA - 05060191070928

Applicator 20 x 6
ELEKTA LIMITED
1525341
In Commercial Distribution

  • 05060191070928 ()


  • Linear accelerator system
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