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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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Tibial insert trial, #5, 9mm
UNITED ORTHOPEDIC CORP.
2303-2251-RK
In Commercial Distribution

  • 04719886892635 ()
2303-2251-RK

  • Knee tibia prosthesis trial, reusable
Tibial baseplate trial, NON-CEM, #5
UNITED ORTHOPEDIC CORP.
2203-4650
In Commercial Distribution

  • 04719886891249 ()
2203-4650

  • Knee tibia prosthesis trial, reusable
Tibial Baseplate, STD, PF+, #5
UNITED ORTHOPEDIC CORP.
2203-3650
In Commercial Distribution

  • 04719886890891 ()


  • Cruciate-retaining total knee prosthesis
  • Posterior-stabilized total knee prosthesis
Hinge box trial, R, #5
UNITED ORTHOPEDIC CORP.
9325-5725
In Commercial Distribution

  • 04719886907131 ()
9325-5725

  • Knee femur prosthesis trial, reusable
Hinge box trial, L, #5
UNITED ORTHOPEDIC CORP.
9325-5715
In Commercial Distribution

  • 04719886907070 ()
9325-5715

  • 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
PSA Box trial, R, #5
UNITED ORTHOPEDIC CORP.
9323-5525
In Commercial Distribution

  • 04719886907018 ()
9323-5525

  • Knee femur prosthesis trial, reusable
PSA Box trial, L, #5
UNITED ORTHOPEDIC CORP.
9323-5515
In Commercial Distribution

  • 04719886906967 ()
9323-5515

  • Knee femur prosthesis trial, reusable
Tibial punch, NON-CEM, #3~#5
UNITED ORTHOPEDIC CORP.
9404-6402
In Commercial Distribution

  • 04719886892161 ()
9404-6402

  • Orthopaedic broach
Tibial Baseplate, Long, PF+, #5
UNITED ORTHOPEDIC CORP.
2203-3750
In Commercial Distribution

  • 04719886890969 ()


  • Cruciate-retaining total knee prosthesis
  • Posterior-stabilized total knee prosthesis
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