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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 28 ID 58-60 OD 20 DEG SIZE G
Smith & Nephew, Inc.
71742858
In Commercial Distribution

  • 03596010232281 ()
71742858

  • Acetabulum prosthesis trial, prefabricated, reusable
REFLECTION LINER 26 ID 70-76 OD 20 DEG SIZE K
Smith & Nephew, Inc.
71742670
In Commercial Distribution

  • 03596010232243 ()
71742670

  • Acetabulum prosthesis trial, prefabricated, reusable
REFLECTION LINER 26 ID 62-64 OD 20 DEG SIZE H
Smith & Nephew, Inc.
71742662
In Commercial Distribution

  • 03596010232229 ()
71742662

  • Acetabulum prosthesis trial, prefabricated, reusable
REFLECTION LINER 26 ID 58-60 OD 20 DEG SIZE G
Smith & Nephew, Inc.
71742658
In Commercial Distribution

  • 03596010232212 ()
71742658

  • Acetabulum prosthesis trial, prefabricated, reusable
REFLECTION LINER 26 ID 55-56 OD 20 DEG SIZE F
Smith & Nephew, Inc.
71742654
In Commercial Distribution

  • 03596010232205 ()
71742654

  • Acetabulum prosthesis trial, prefabricated, reusable
REFLECTION LINER 26 ID 50-52 OD 20 DEG SIZE E
Smith & Nephew, Inc.
71742650
In Commercial Distribution

  • 03596010232199 ()
71742650

  • Acetabulum prosthesis trial, prefabricated, reusable
REFLECTION LINER 26 ID 46-48 OD 20 DEG SIZE D
Smith & Nephew, Inc.
71742646
In Commercial Distribution

  • 03596010232182 ()
71742646

  • Acetabulum prosthesis trial, prefabricated, reusable
REFLECTION LINER 22 ID 44 OD 20 DEG SIZE C
Smith & Nephew, Inc.
71742244
In Commercial Distribution

  • 03596010232090 ()
71742244

  • Acetabulum prosthesis trial, prefabricated, reusable
REFLECTION LINER 22 ID 42 OD 20 DEG SIZE B
Smith & Nephew, Inc.
71742242
In Commercial Distribution

  • 03596010232083 ()
71742242

  • Acetabulum prosthesis trial, prefabricated, reusable
Dual Hole Foot Ring Short, 210mm ID, Aluminum, Purple, Non-Sterile
Wishbone Medical, Inc.
10-700-21058UA-0
Not in Commercial Distribution

  • B5621070021058UA00 ()
10-700-21058UA-0

  • General external orthopaedic fixation system implantation kit, single-use
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