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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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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
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
No Description
Bauerfeind AG
21215011520009
In Commercial Distribution

  • 04046445897603 ()


  • Compression/pressure sock/stocking, single-use
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