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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, PS, #0, 9mm
UNITED ORTHOPEDIC CORP.
2303-4001
In Commercial Distribution

  • 04719872164487 ()

  • PS, #0, 9mm
2303-4001

  • Knee tibia prosthesis trial, reusable
Tibial insert trial, UC, #0, 18mm
UNITED ORTHOPEDIC CORP.
2303-2405-RF
In Commercial Distribution

  • 04719872163770 ()
2303-2405-RF

  • Knee tibia prosthesis trial, reusable
Tibial insert trial, UC, #0, 15mm
UNITED ORTHOPEDIC CORP.
2303-2404-RF
In Commercial Distribution

  • 04719872163756 ()
2303-2404-RF

  • Knee tibia prosthesis trial, reusable
Tibial insert trial, UC, #0, 13mm
UNITED ORTHOPEDIC CORP.
2303-2403-RF
In Commercial Distribution

  • 04719872163732 ()
2303-2403-RF

  • Knee tibia prosthesis trial, reusable
Tibial insert trial, UC, #0, 11mm
UNITED ORTHOPEDIC CORP.
2303-2402-RF
In Commercial Distribution

  • 04719872163718 ()
2303-2402-RF

  • Knee tibia prosthesis trial, reusable
Tibial insert trial, UC, #0, 9mm
UNITED ORTHOPEDIC CORP.
2303-2401-RF
In Commercial Distribution

  • 04719872163695 ()
2303-2401-RF

  • Knee tibia prosthesis trial, reusable
Cervical IBF-SW, PEEK, 14x11, 0°, 10mm
VY SPINE LLC
1-SW02-010
In Commercial Distribution

  • 00842566101971 ()
1-SW02-010

  • Polymeric spinal interbody fusion cage
Cervical IBF-SW, PEEK, 14x11, 0°, 8mm
VY SPINE LLC
1-SW02-008
In Commercial Distribution

  • 00842566101957 ()
1-SW02-008

  • Polymeric spinal interbody fusion cage
Cervical IBF-SW, PEEK, 14x11, 0°, 4mm
VY SPINE LLC
1-SW02-004
In Commercial Distribution

  • 00842566101919 ()
1-SW02-004

  • Polymeric spinal interbody fusion cage
Cervical IBF-SL, PEEK, 14x11, 0°, 11mm
VY SPINE LLC
1-SL02-011
In Commercial Distribution

  • 00842566101827 ()
1-SL02-011

  • Polymeric spinal interbody fusion cage
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