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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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CROSSFUSE II HYPERLORDOTIC LH ANG INSRTR
Rti Surgical, Inc.
724-419
In Commercial Distribution

  • 00191083027371 ()
724-419

  • Orthopaedic inorganic implant inserter/extractor, reusable
LAT FUS, LG BAYONETTED RASP, UP BEND
Rti Surgical, Inc.
724-366
In Commercial Distribution

  • 00191083027326 ()
724-366

  • General internal orthopaedic fixation system implantation kit
LAT FUS, LG BAYONET RING CUR , STRAIGHT
Rti Surgical, Inc.
724-363
In Commercial Distribution

  • 00191083027302 ()
724-363

  • Bone curette, reusable
LAT FUS, MED BAYONETTED COBB, STRAIGHT
Rti Surgical, Inc.
724-361
In Commercial Distribution

  • 00191083027289 ()
724-361

  • General internal orthopaedic fixation system implantation kit
SHARED SPINE, 5mm INITIATOR
Rti Surgical, Inc.
724-297
In Commercial Distribution

  • 00191083027265 ()
724-297

  • General internal orthopaedic fixation system implantation kit
CLARITY LATERAL, 3 BLADE RG RETRACTOR
Rti Surgical, Inc.
724-175
In Commercial Distribution

  • 00191083027258 ()
724-175

  • Surgical retraction system, reusable
CLARITY LATERAL, 3 BLADE RETRACTOR
Rti Surgical, Inc.
724-028
In Commercial Distribution

  • 00191083027241 ()
724-028

  • Surgical retraction system, reusable
LAT FUS, 5 DEG DOWN BEND COBB-S
Rti Surgical, Inc.
723-785
In Commercial Distribution

  • 00191083027227 ()
723-785

  • General internal orthopaedic fixation system implantation kit
30mm CLARITY POSTERIOR BLADE,90deg
Rti Surgical, Inc.
723-679
In Commercial Distribution

  • 00191083027210 ()
723-679

  • Surgical retraction system, reusable
40mm CLARITY POSTERIOR BLADE,90deg
Rti Surgical, Inc.
723-678
In Commercial Distribution

  • 00191083027203 ()
723-678

  • Surgical retraction system, reusable
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