SEARCH RESULTS FOR: ("apk報毒處理[Contact Telegram: crmeb8].lbk")(11932 results)

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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 CRUCIATE RETAINING POROUS FEMORAL SIZE 1 RIGHT
Smith & Nephew, Inc.
71420048
In Commercial Distribution

  • 03596010205674 ()
71420048

  • Knee arthroplasty wedge
GENESIS II CRUCIATE RETAINING POROUS FEMORAL SIZE 8 LEFT
Smith & Nephew, Inc.
71420046
In Commercial Distribution

  • 03596010205667 ()
71420046

  • Knee arthroplasty wedge
GENESIS II CRUCIATE RETAINING POROUS FEMORAL SIZE 7 LEFT
Smith & Nephew, Inc.
71420044
In Commercial Distribution

  • 03596010205650 ()
71420044

  • Knee arthroplasty wedge
GENESIS II CRUCIATE RETAINING POROUS FEMORAL SIZE 6 LEFT
Smith & Nephew, Inc.
71420042
In Commercial Distribution

  • 03596010205643 ()
71420042

  • Knee arthroplasty wedge
GENESIS II CRUCIATE RETAINING POROUS FEMORAL SIZE 5 LEFT
Smith & Nephew, Inc.
71420040
In Commercial Distribution

  • 03596010205636 ()
71420040

  • Knee arthroplasty wedge
GENESIS II CRUCIATE RETAINING POROUS FEMORAL SIZE 4 LEFT
Smith & Nephew, Inc.
71420038
In Commercial Distribution

  • 03596010205629 ()
71420038

  • Knee arthroplasty wedge
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
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