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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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PSA Femoral cut through trial, #5
UNITED ORTHOPEDIC CORP.
2123-6150
In Commercial Distribution

  • 04719886905588 ()
2123-6150

  • Knee femur prosthesis trial, reusable
Femoal spacer sizing template, #4~#5
UNITED ORTHOPEDIC CORP.
9909-7414
In Commercial Distribution

  • 04719886901757 ()
9909-7414

  • Surgical implant template, reusable
Femoral distal augment trial, #5, 16mm
UNITED ORTHOPEDIC CORP.
2623-6354
In Commercial Distribution

  • 04719886907643 ()
2623-6354

  • Knee femur prosthesis trial, reusable
Femoral distal augment trial, #5, 12mm
UNITED ORTHOPEDIC CORP.
2623-6353
In Commercial Distribution

  • 04719886907636 ()
2623-6353

  • Knee femur prosthesis trial, reusable
Femoral distal augment trial, #5, 8mm
UNITED ORTHOPEDIC CORP.
2623-6352
In Commercial Distribution

  • 04719886907629 ()
2623-6352

  • Knee femur prosthesis trial, reusable
Femoral distal augment trial, #5, 4mm
UNITED ORTHOPEDIC CORP.
2623-6351
In Commercial Distribution

  • 04719886907612 ()
2623-6351

  • Knee femur prosthesis trial, reusable
Femoral posterior augment trial, #5, 8mm
UNITED ORTHOPEDIC CORP.
2623-6052
In Commercial Distribution

  • 04719886907315 ()
2623-6052

  • Knee femur prosthesis trial, reusable
Femoral posterior augment trial, #5, 4mm
UNITED ORTHOPEDIC CORP.
2623-6051
In Commercial Distribution

  • 04719886907254 ()
2623-6051

  • Knee femur prosthesis trial, reusable
Tibial insert trial, PSA, #5, 13mm
UNITED ORTHOPEDIC CORP.
2323-6053
In Commercial Distribution

  • 04719886905946 ()
2323-6053

  • Knee tibia prosthesis trial, reusable
Tibial insert trial, PSA, #5, 9mm
UNITED ORTHOPEDIC CORP.
2323-6051
In Commercial Distribution

  • 04719886905922 ()
2323-6051

  • Knee tibia prosthesis trial, reusable
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