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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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No Description
Biomet Orthopedics, LLC
467265
In Commercial Distribution

  • 00880304380660 ()
  • 70880304380669 ()

  • 60CM (L) - PK/2
467265

  • Cannulated surgical drill guiding pin
No Description
BIOPRO, INC.
22648
In Commercial Distribution

  • 00810012485869 ()


  • Orthopaedic bone wire
No Description
BIOPRO, INC.
22647
In Commercial Distribution

  • 00810012485852 ()


  • Orthopaedic bone wire
No Description
BIOPRO, INC.
22646
In Commercial Distribution

  • 00810012485845 ()


  • Orthopaedic bone wire
No Description
BIOPRO, INC.
22645
In Commercial Distribution

  • 00810012485838 ()


  • Orthopaedic bone wire
No Description
BIOPRO, INC.
22644
In Commercial Distribution

  • 00810012485821 ()


  • Orthopaedic bone wire
This device is intended for use during cardiopulmonary bypass in conjunction with other medically approved devices and equipment that are utilized for this procedure.
Cardiomed Supplies Inc
1.4
In Commercial Distribution

  • 16641670004281 ()
  • 36641670004292 ()
C-666

  • Low-pressure tubing connector, single-use, sterile
No Description
BIOMET SPINE LLC
7740-8570
In Commercial Distribution

  • 00888480545552 ()

  • CANN POLY DUAL LEAD PED SCW TI 8.5X70MM
7740-8570

  • Bone-screw internal spinal fixation system, non-sterile
No Description
BIOMET SPINE LLC
7740-8565
In Commercial Distribution

  • 00888480545545 ()

  • CANN POLY DUAL LEAD PED SCW TI 8.5X65MM
7740-8565

  • Bone-screw internal spinal fixation system, non-sterile
No Description
BIOMET SPINE LLC
7740-8560
In Commercial Distribution

  • 00888480545538 ()

  • CANN POLY DUAL LEAD PED SCW TI 8.5X60MM
7740-8560

  • Bone-screw internal spinal fixation system, non-sterile
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