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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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ENDO-EAR Suction, Straight, 20 Ga
Mytamed, Inc.
1.80.20
Not in Commercial Distribution

  • B351180200 ()
1.80.20

  • Surgical/emergency suction cannula, non-illuminating, reusable
MCP, Broach, Proximal, Sz. 20
Ascension Orthopedics, Inc.
BRH10020P
In Commercial Distribution

  • M269BRH10020P1 ()
  • 10381780242222 ()

  • Size 20
BRH-100-20P

  • Orthopaedic broach
MCP, Broach, Distal, Sz. 20
Ascension Orthopedics, Inc.
BRH10020D
In Commercial Distribution

  • M269BRH10020D1 ()
  • 10381780242215 ()

  • Size 20
BRH-100-20D

  • Orthopaedic broach
Trial Augment 70/72 20
Medacta International SA
01.38.10.7020
In Commercial Distribution

  • 07630040761017 ()


  • Orthopaedic surgical procedure kit, non-medicated, reusable
Trial Augment 66/68 20
Medacta International SA
01.38.10.6620
In Commercial Distribution

  • 07630040760980 ()


  • Orthopaedic surgical procedure kit, non-medicated, reusable
Trial Augment 62/64 20
Medacta International SA
01.38.10.6220
In Commercial Distribution

  • 07630040760959 ()


  • Orthopaedic surgical procedure kit, non-medicated, reusable
Trial Augment 58/60 20
Medacta International SA
01.38.10.5820
In Commercial Distribution

  • 07630040760928 ()


  • Orthopaedic surgical procedure kit, non-medicated, reusable
Trial Augment 54/56 20
Medacta International SA
01.38.10.5420
In Commercial Distribution

  • 07630040760898 ()


  • Orthopaedic surgical procedure kit, non-medicated, reusable
Trial Augment 50/52 20
Medacta International SA
01.38.10.5020
In Commercial Distribution

  • 07630040760867 ()


  • Orthopaedic surgical procedure kit, non-medicated, reusable
NEUFLEX MCP TRIAL SIZE 20
DEPUY ORTHOPAEDICS, INC.
2634-20-000
Not in Commercial Distribution

  • 10603295149668 ()
263420000

  • Surgical implant template, reusable
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