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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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REFLECTION LINER 32 ID 70-76 OD 0 DEG SIZE K
Smith & Nephew, Inc.
71740270
In Commercial Distribution

  • 03596010231826 ()
71740270

  • Acetabulum prosthesis trial, prefabricated, reusable
REFLECTION LINER 32 ID 50-52 OD 0 DEG SIZE E
Smith & Nephew, Inc.
71740250
In Commercial Distribution

  • 03596010231772 ()
71740250

  • Acetabulum prosthesis trial, prefabricated, reusable
REFLECTION LINER 32 ID 70-76 OD 20 DEG SIZE K
Smith & Nephew, Inc.
71743270
In Commercial Distribution

  • 03596010232373 ()
71743270

  • Acetabulum prosthesis trial, prefabricated, reusable
REFLECTION LINER 32 ID 66-68 OD 20 DEG SIZE J
Smith & Nephew, Inc.
71743266
In Commercial Distribution

  • 03596010232366 ()
71743266

  • Acetabulum prosthesis trial, prefabricated, reusable
REFLECTION LINER 28 ID 70-76 OD 20 DEG SIZE K
Smith & Nephew, Inc.
71742870
In Commercial Distribution

  • 03596010232311 ()
71742870

  • Acetabulum prosthesis trial, prefabricated, reusable
REFL ACET LINER 28MM ID X 70MM W/35DEG LIP
Smith & Nephew, Inc.
71923737
Not in Commercial Distribution

  • 03596010427946 ()
71923737

  • Ceramic acetabular liner
REFL ACET LINER 28MM ID X 66-68MM W/35DEG LIP
Smith & Nephew, Inc.
71923736
Not in Commercial Distribution

  • 03596010427939 ()
71923736

  • Ceramic acetabular liner
REFL ACET LINER 28MM ID X 62-64MM W/35DEG LIP
Smith & Nephew, Inc.
71923735
Not in Commercial Distribution

  • 03596010427922 ()
71923735

  • Ceramic acetabular liner
REFL ACET LINER 28MM ID X 46-48MM W/35DEG LIP
Smith & Nephew, Inc.
71923734
In Commercial Distribution

  • 03596010427915 ()
71923734

  • Ceramic acetabular liner
SPRING NITI OPEN COIL SPOOL 400G 018 063 ID 15"
AMERICAN ORTHODONTICS CORPORATION
855-617
In Commercial Distribution

  • 00190746075636 ()
855-617

  • Orthodontic spring
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