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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 baseplate trial, #5
UNITED ORTHOPEDIC CORP.
2203-4050-RB
In Commercial Distribution

  • 04719872168850 ()

  • #5
2203-4050-RB

  • Patella prosthesis trial
Tibial baseplate trial, #5
UNITED ORTHOPEDIC CORP.
2203-4050-RA
In Commercial Distribution

  • 04719872168843 ()

  • #5
2203-4050-RA

  • Knee tibia prosthesis trial, reusable
Tibial spacer base, #5
UNITED ORTHOPEDIC CORP.
9403-7350
In Commercial Distribution

  • 04719872167761 ()

  • #5
9403-7350

  • Knee tibia prosthesis trial, reusable
MIS femoral A/P chamfer cutting guide,#5
UNITED ORTHOPEDIC CORP.
9303-2551
In Commercial Distribution

  • 04719872167730 ()

  • #5
9303-2551

  • Osteotomy guide, reusable
U2 Broach, #5
UNITED ORTHOPEDIC CORP.
9104-6050-RB
In Commercial Distribution

  • 04719872167037 ()

  • #5
9104-6050-RB

  • Orthopaedic broach
U2 Broach, #5
UNITED ORTHOPEDIC CORP.
9104-6050-RA
In Commercial Distribution

  • 04719872167020 ()

  • #5
9104-6050-RA

  • Orthopaedic broach
U2 Broach, #5
UNITED ORTHOPEDIC CORP.
9104-6050
In Commercial Distribution

  • 04719872167013 ()

  • #5
9104-6050

  • Orthopaedic broach
Tibial sizing template, #5
UNITED ORTHOPEDIC CORP.
9403-7305
In Commercial Distribution

  • 04719872158400 ()

  • #5
9403-7305

  • Surgical implant template, reusable
Femoral sizing template, #5
UNITED ORTHOPEDIC CORP.
9303-7315-RT
In Commercial Distribution

  • 04719872158318 ()

  • #5
9303-7315-RT

  • Surgical implant template, reusable
Femoral sizing template, #5
UNITED ORTHOPEDIC CORP.
9303-7315-RB
In Commercial Distribution

  • 04719872158301 ()

  • #5
9303-7315-RB

  • Surgical implant template, reusable
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