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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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GENESIS II C/R POROUS FEMORAL SIZE 3 LEFT
Smith & Nephew, Inc.
71420036
In Commercial Distribution

  • 03596010205612 ()
71420036

  • Knee arthroplasty wedge
GENESIS II CRUCIATE RETAINING POROUS FEMORAL SIZE 2 LEFT
Smith & Nephew, Inc.
71420034
In Commercial Distribution

  • 03596010205605 ()
71420034

  • Knee arthroplasty wedge
GENESIS II CRUCIATE RETAINING POROUS FEMORAL SIZE 1 LEFT
Smith & Nephew, Inc.
71420032
In Commercial Distribution

  • 03596010205599 ()
71420032

  • Knee arthroplasty wedge
GENESIS II NON POROUS CRUCIATE RETAINING FEMORAL SIZE 8 RIGHT
Smith & Nephew, Inc.
71420030
In Commercial Distribution

  • 03596010205582 ()
71420030

  • Knee arthroplasty wedge
GENESIS II NON-POROUS C/R FEMORAL SIZE 7 RIGHT
Smith & Nephew, Inc.
71420028
In Commercial Distribution

  • 03596010205575 ()
71420028

  • Knee arthroplasty wedge
GENESIS II NON POROUS CRUCIATE RETAINING FEMORAL SIZE 6 RIGHT
Smith & Nephew, Inc.
71420026
In Commercial Distribution

  • 03596010205568 ()
71420026

  • Knee arthroplasty wedge
GENESIS II NON POROUS C/R FEMORAL SIZE 5 RIGHT
Smith & Nephew, Inc.
71420024
In Commercial Distribution

  • 03596010205551 ()
71420024

  • Knee arthroplasty wedge
GENESIS II NON POROUS CRUCIATE RETAINING FEMORAL SIZE 4 RIGHT
Smith & Nephew, Inc.
71420022
In Commercial Distribution

  • 03596010205544 ()
71420022

  • Knee arthroplasty wedge
GENESIS II NON POROUS C/R FEMORAL SIZE 3 RIGHT
Smith & Nephew, Inc.
71420020
In Commercial Distribution

  • 03596010205537 ()
71420020

  • Knee arthroplasty wedge
GENESIS II NON POROUS CRUCIATE RETAINING FEMORAL SIZE 2 RIGHT
Smith & Nephew, Inc.
71420018
In Commercial Distribution

  • 03596010205520 ()
71420018

  • Knee arthroplasty wedge
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