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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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Femoral A/P chamfer cutting guide, #5
UNITED ORTHOPEDIC CORP.
9303-2150-RC
In Commercial Distribution

  • 04719872157359 ()

  • #5
9303-2150-RC

  • Osteotomy guide, reusable
Femoral A\ P chamfer cutting guide ,#5
UNITED ORTHOPEDIC CORP.
9303-2150-RA
In Commercial Distribution

  • 04719872157342 ()

  • #5
9303-2150-RA

  • Osteotomy guide, reusable
Femoral A/P chamfer cutting guide, #5
UNITED ORTHOPEDIC CORP.
9303-2150
In Commercial Distribution

  • 04719872157335 ()

  • #5
9303-2150

  • Osteotomy guide, reusable
UCP Stem broach, #5
UNITED ORTHOPEDIC CORP.
9107-6050
In Commercial Distribution

  • 04719872157069 ()

  • #5
9107-6050

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

  • 04719872156819 ()

  • #5
9104-6050-RC

  • Orthopaedic broach
Neck trial, #5
UNITED ORTHOPEDIC CORP.
9104-5004-RB
In Commercial Distribution

  • 04719872171034 ()

  • #5
9104-5004-RB

  • Femoral stem prosthesis trial
Neck trial, #5
UNITED ORTHOPEDIC CORP.
9104-5004
In Commercial Distribution

  • 04719872171027 ()

  • #5
9104-5004

  • Femoral stem prosthesis trial
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
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