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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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ATTUNE KNEE SYSTEM REVISION TIBIAL AUGMENT 10MM RM/LL CEMENTED SIZE 1/2
DEPUY (IRELAND)
1523-01-202
In Commercial Distribution

  • 10603295057529 ()
152301202

  • Knee arthroplasty wedge
ATTUNE KNEE SYSTEM REVISION TIBIAL AUGMENT 10MM LM/RL CEMENTED SIZE 1/2
DEPUY (IRELAND)
1523-01-102
In Commercial Distribution

  • 10603295057505 ()
152301102

  • Knee arthroplasty wedge
LCS COMPLETE POSTERIOR AUGMENT 10mm LG+
DEPUY ORTHOPAEDICS, INC.
1294-27-071
In Commercial Distribution

  • 10603295025412 ()
129427071

  • Knee arthroplasty wedge
LCS COMPLETE POSTERIOR AUGMENT 5mm LG+
DEPUY ORTHOPAEDICS, INC.
1294-27-070
In Commercial Distribution

  • 10603295025405 ()
129427070

  • Knee arthroplasty wedge
LCS COMPLETE POSTERIOR AUGMENT 10mm LG
DEPUY ORTHOPAEDICS, INC.
1294-27-061
In Commercial Distribution

  • 10603295025399 ()
129427061

  • Knee arthroplasty wedge
LCS COMPLETE POSTERIOR AUGMENT 5mm LG
DEPUY ORTHOPAEDICS, INC.
1294-27-060
In Commercial Distribution

  • 10603295025382 ()
129427060

  • Knee arthroplasty wedge
LCS COMPLETE POSTERIOR AUGMENT 10mm STD+
DEPUY ORTHOPAEDICS, INC.
1294-27-051
In Commercial Distribution

  • 10603295025375 ()
129427051

  • Knee arthroplasty wedge
LCS COMPLETE POSTERIOR AUGMENT 5mm STD+
DEPUY ORTHOPAEDICS, INC.
1294-27-050
In Commercial Distribution

  • 10603295025368 ()
129427050

  • Knee arthroplasty wedge
LCS COMPLETE POSTERIOR AUGMENT 10mm STD
DEPUY ORTHOPAEDICS, INC.
1294-27-041
In Commercial Distribution

  • 10603295025351 ()
129427041

  • Knee arthroplasty wedge
LCS COMPLETE POSTERIOR AUGMENT 5mm STD
DEPUY ORTHOPAEDICS, INC.
1294-27-040
In Commercial Distribution

  • 10603295025344 ()
129427040

  • Knee arthroplasty wedge
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