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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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CURETTE BRUN 9" HEXAGON HNDL ANG #0
TELEFLEX INCORPORATED
IPN911981
In Commercial Distribution

  • 54026704796583 ()
  • 14026704796585 ()
P20652

  • Neurosurgical curette, single-use
CURETTE SPINAL FUSION FLAT SZ 3 9"
TELEFLEX INCORPORATED
IPN019246
In Commercial Distribution

  • 54026704796538 ()
  • 14026704796530 ()
P20581

  • Neurosurgical curette, single-use
CURETTE SPINAL DUSION FLAT SZ 2 9"
TELEFLEX INCORPORATED
IPN019244
In Commercial Distribution

  • 54026704796514 ()
  • 14026704796516 ()
P20579

  • Neurosurgical curette, single-use
CURETTE SPINAL FUSION FLAT SZ 1 9"
TELEFLEX INCORPORATED
IPN019242
In Commercial Distribution

  • 54026704796491 ()
  • 14026704796493 ()
P20577

  • Neurosurgical curette, single-use
CURETTE SPINAL FUSION FLAT SZ 0 9"
TELEFLEX INCORPORATED
IPN019240
In Commercial Distribution

  • 54026704796477 ()
  • 14026704796479 ()
P20575

  • Neurosurgical curette, single-use
CURETTE SPINAL REV ANG SZ 0 9"
TELEFLEX INCORPORATED
IPN019239
In Commercial Distribution

  • 54026704796460 ()
  • 14026704796462 ()
P20574

  • Bone curette, reusable
CURETTE SPINAL REV ANG SZ 2-0 9"
TELEFLEX INCORPORATED
IPN019237
In Commercial Distribution

  • 54026704796446 ()
  • 14026704796448 ()
P20572

  • Bone curette, reusable
CURETTE SPINAL REV ANG SZ 3-0 9"
TELEFLEX INCORPORATED
IPN019235
In Commercial Distribution

  • 54026704796439 ()
  • 14026704796431 ()
P20570

  • Bone curette, reusable
CURETTE SPINAL FUSHION ANG SZ 0 9"
TELEFLEX INCORPORATED
IPN019225
In Commercial Distribution

  • 54026704796408 ()
  • 14026704796400 ()
P20527

  • Neurosurgical curette, single-use
CURETTE SPINAL FUSHION ANG SZ 2-0 9"
TELEFLEX INCORPORATED
IPN019224
In Commercial Distribution

  • 54026704796392 ()
  • 14026704796394 ()
P20525

  • Neurosurgical curette, single-use
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