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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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50mm CLARITY POSTERIOR BLADE,90deg
Rti Surgical, Inc.
723-677
In Commercial Distribution

  • 00191083027197 ()
723-677

  • Surgical retraction system, reusable
60mm CLARITY POSTERIOR BLADE,90deg
Rti Surgical, Inc.
723-676
In Commercial Distribution

  • 00191083027180 ()
723-676

  • Surgical retraction system, reusable
70mm CLARITY POSTERIOR BLADE,90deg
Rti Surgical, Inc.
723-675
In Commercial Distribution

  • 00191083027173 ()
723-675

  • Surgical retraction system, reusable
FUSION, 15in DBL SIDED RASP, 5mmx8mm
Rti Surgical, Inc.
723-553
In Commercial Distribution

  • 00191083027166 ()
723-553

  • General internal orthopaedic fixation system implantation kit
FUSION, 14in SIDE BEND RING CURETTE, 8mm
Rti Surgical, Inc.
723-551
In Commercial Distribution

  • 00191083027159 ()
723-551

  • Bone curette, reusable
FUSION, 14in STRAIGHT RING CURETTE, 8mm
Rti Surgical, Inc.
723-550
In Commercial Distribution

  • 00191083027142 ()
723-550

  • Bone curette, reusable
FUSION, 14in EPSTEIN CURETTE, SIZE 2
Rti Surgical, Inc.
723-549
In Commercial Distribution

  • 00191083027135 ()
723-549

  • Bone curette, reusable
FUSION, 15in STRAIGHT CURETTE, SIZE 2
Rti Surgical, Inc.
723-547
In Commercial Distribution

  • 00191083027111 ()
723-547

  • Bone curette, reusable
CROSSFUSE II, 22mm FORKED TAMP, 15 degree BEND
Rti Surgical, Inc.
723-478
In Commercial Distribution

  • 00191083027081 ()
723-478

  • General internal orthopaedic fixation system implantation kit
CROSFUSE II, TAMP, 15 degree BEND
Rti Surgical, Inc.
723-476
In Commercial Distribution

  • 00191083027067 ()
723-476

  • General internal orthopaedic fixation system implantation kit
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