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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VIPER 2 SYSTEM INTERMEDIATE DRIVER, SELF-RETAINING 5.5 X-25
DEPUY SPINE, LLC
286735430
In Commercial Distribution

  • 10705034214603 ()
286735430

  • Orthopaedic implant driver
VIPER 2 SYSTEM CASTLE NUT TIGHTENER
DEPUY SPINE, LLC
286725400
In Commercial Distribution

  • 10705034214375 ()
286725400

  • Orthopaedic implant driver
VIPER 2 SYSTEM DRIVER, CANNULATED T20
DEPUY SPINE, LLC
286725020
In Commercial Distribution

  • 10705034214290 ()
286725020

  • Orthopaedic implant driver
VIPER 2 SYSTEM HEXLOBE ROD TIGHTENER SHAFT x15
DEPUY SPINE, LLC
286725010
In Commercial Distribution

  • 10705034214283 ()
286725010

  • Orthopaedic implant driver
VIPER SYSTEM CASTLE NUT TIGHTENER
DEPUY SPINE, LLC
286720400
In Commercial Distribution

  • 10705034214269 ()
286720400

  • Orthopaedic implant driver
EXPEDIUM and VIPER 2 SPINE SYSTEM CANNULATED - MONOAXIAL DRIVER
DEPUY SPINE, LLC
286720100
In Commercial Distribution

  • 10705034214214 ()
286720100

  • Orthopaedic implant driver
VIPER SYSTEM DRIVER SHAFT, CANNULATED T20
DEPUY SPINE, LLC
286720020
In Commercial Distribution

  • 10705034214207 ()
286720020

  • Orthopaedic implant driver
VIPER SYSTEM HEXLOBE ROD TIGHTENER X15
DEPUY SPINE, LLC
286720015
In Commercial Distribution

  • 10705034214191 ()
286720015

  • Orthopaedic implant driver
VIPER SYSTEM HEXLOBE ROD TIGHTENER x15
DEPUY SPINE, LLC
286720010
In Commercial Distribution

  • 10705034214184 ()
286720010

  • Orthopaedic implant driver
VIPER SYSTEM POLY SCREWDRIVER SHAFT, CANN.
Medos International Sàrl
286720000
In Commercial Distribution

  • 10705034214177 ()
286720000

  • Orthopaedic implant driver
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