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 Class Implantable

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2MM RECUT BLOCK
Smith & Nephew, Inc.
E0018008-1
In Commercial Distribution

  • 00885556899953 ()
E0018008-1

  • Osteotomy guide, reusable
SZ 10 MEDIAL TIBIA IMPLANT TRIAL - RT
Smith & Nephew, Inc.
E0017895-20
In Commercial Distribution

  • 00885556889404 ()
E0017895-20

  • Knee tibia prosthesis trial, reusable
SZ 9 MEDIAL TIBIA IMPLANT TRIAL - RT
Smith & Nephew, Inc.
E0017895-19
In Commercial Distribution

  • 00885556889398 ()
E0017895-19

  • Knee tibia prosthesis trial, reusable
SZ 8 MEDIAL TIBIA IMPLANT TRIAL - RT
Smith & Nephew, Inc.
E0017895-18
In Commercial Distribution

  • 00885556889381 ()
E0017895-18

  • Knee tibia prosthesis trial, reusable
SZ 7 MEDIAL TIBIA IMPLANT TRIAL - RT
Smith & Nephew, Inc.
E0017895-17
In Commercial Distribution

  • 00885556889374 ()
E0017895-17

  • Knee tibia prosthesis trial, reusable
SZ 6 MEDIAL TIBIA IMPLANT TRIAL - RT
Smith & Nephew, Inc.
E0017895-16
In Commercial Distribution

  • 00885556889367 ()
E0017895-16

  • Knee tibia prosthesis trial, reusable
SZ 5 MEDIAL TIBIA IMPLANT TRIAL - RT
Smith & Nephew, Inc.
E0017895-15
In Commercial Distribution

  • 00885556889350 ()
E0017895-15

  • Knee tibia prosthesis trial, reusable
SZ 4 MEDIAL TIBIA IMPLANT TRIAL - RT
Smith & Nephew, Inc.
E0017895-14
In Commercial Distribution

  • 00885556889343 ()
E0017895-14

  • Knee tibia prosthesis trial, reusable
SZ 3 MEDIAL TIBIA IMPLANT TRIAL - RT
Smith & Nephew, Inc.
E0017895-13
In Commercial Distribution

  • 00885556889336 ()
E0017895-13

  • Knee tibia prosthesis trial, reusable
SZ 2 MEDIAL TIBIA IMPLANT TRIAL - RT
Smith & Nephew, Inc.
E0017895-12
In Commercial Distribution

  • 00885556889329 ()
E0017895-12

  • Knee tibia prosthesis trial, reusable
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