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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, Size 16x20x8 mm, 0°
K2M, INC.
402-90554
In Commercial Distribution

  • 10888857314528 ()
402-90554

  • General internal orthopaedic fixation system implantation kit
Trial, Size 16x20x6 mm, 0°
K2M, INC.
402-90552
In Commercial Distribution

  • 10888857314504 ()
402-90552

  • General internal orthopaedic fixation system implantation kit
Trial, Size 16x20x5 mm, 0°
K2M, INC.
402-90551
In Commercial Distribution

  • 10888857314498 ()
402-90551

  • General internal orthopaedic fixation system implantation kit
Convex Trial, Size 16x20x15 mm
K2M, INC.
402-90550
In Commercial Distribution

  • 10888857314481 ()
402-90550

  • General internal orthopaedic fixation system implantation kit
Convex Trial, Size 16x20x14 mm
K2M, INC.
402-90549
In Commercial Distribution

  • 10888857314474 ()
402-90549

  • General internal orthopaedic fixation system implantation kit
Convex Trial, Size 16x20x13 mm
K2M, INC.
402-90548
In Commercial Distribution

  • 10888857314467 ()
402-90548

  • General internal orthopaedic fixation system implantation kit
Convex Trial, Size 16x20x11 mm
K2M, INC.
402-90546
In Commercial Distribution

  • 10888857314443 ()
402-90546

  • General internal orthopaedic fixation system implantation kit
Convex Trial, Size 16x20x10 mm
K2M, INC.
402-90545
In Commercial Distribution

  • 10888857314436 ()
402-90545

  • General internal orthopaedic fixation system implantation kit
Convex Trial, Size 16x20x9 mm
K2M, INC.
402-90544
In Commercial Distribution

  • 10888857314429 ()
402-90544

  • General internal orthopaedic fixation system implantation kit
Convex Trial, Size 16x20x8 mm
K2M, INC.
402-90543
In Commercial Distribution

  • 10888857314412 ()
402-90543

  • General internal orthopaedic fixation system implantation kit
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