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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 Box trial, L, #5
UNITED ORTHOPEDIC CORP.
9323-5515
In Commercial Distribution

  • 04719886906967 ()
9323-5515

  • Knee femur prosthesis trial, reusable
PSA Tibial baseplate trial, #5
UNITED ORTHOPEDIC CORP.
2223-6050
In Commercial Distribution

  • 04719886906127 ()
2223-6050

  • Knee tibia prosthesis trial, reusable
Tibial baseplate trial, #5, right
UNITED ORTHOPEDIC CORP.
2203-4250-RG
In Commercial Distribution

  • 04719886894455 ()
2203-4250-RG

  • Knee tibia prosthesis trial, reusable
Tibial baseplate trial, #5, left
UNITED ORTHOPEDIC CORP.
2203-4150-RG
In Commercial Distribution

  • 04719886894394 ()
2203-4150-RG

  • Knee tibia prosthesis trial, reusable
Tibial insert trial, #5, 12mm
UNITED ORTHOPEDIC CORP.
2303-2257-RK
In Commercial Distribution

  • 04719886892697 ()
2303-2257-RK

  • Knee tibia prosthesis trial, reusable
Tibial insert trial, #5, 10mm
UNITED ORTHOPEDIC CORP.
2303-2256-RK
In Commercial Distribution

  • 04719886892680 ()
2303-2256-RK

  • Knee tibia prosthesis trial, reusable
Tibial insert trial, #5, 18mm
UNITED ORTHOPEDIC CORP.
2303-2255-RK
In Commercial Distribution

  • 04719886892673 ()
2303-2255-RK

  • Knee tibia prosthesis trial, reusable
Tibial insert trial, #5, 15mm
UNITED ORTHOPEDIC CORP.
2303-2254-RK
In Commercial Distribution

  • 04719886892666 ()
2303-2254-RK

  • Knee tibia prosthesis trial, reusable
Tibial insert trial, #5, 13mm
UNITED ORTHOPEDIC CORP.
2303-2253-RK
In Commercial Distribution

  • 04719886892659 ()
2303-2253-RK

  • Knee tibia prosthesis trial, reusable
Tibial insert trial, #5, 11mm
UNITED ORTHOPEDIC CORP.
2303-2252-RK
In Commercial Distribution

  • 04719886892642 ()
2303-2252-RK

  • Knee tibia prosthesis trial, reusable
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