SEARCH RESULTS FOR: medtronic(15352 results)

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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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DILATOR EX0921005 16.8 MM
MEDTRONIC SOFAMOR DANEK, INC.
EX0921005
In Commercial Distribution

  • 00763000602710 ()


  • Laparoscopic access cannula dilator
DILATOR EX0921004 12.8 MM
MEDTRONIC SOFAMOR DANEK, INC.
EX0921004
In Commercial Distribution

  • 00763000602703 ()


  • Laparoscopic access cannula dilator
BLADE X07213192 LATERAL - L190MM
MEDTRONIC SOFAMOR DANEK, INC.
X07213192
In Commercial Distribution

  • 00763000595692 ()


  • Surgical retraction system, reusable
BLADE X07213191 CRANIAL-CAUDAL L L190MM
MEDTRONIC SOFAMOR DANEK, INC.
X07213191
In Commercial Distribution

  • 00763000595685 ()


  • Surgical retraction system, reusable
BLADE X07213190 CRANIAL-CAUDAL R L190MM
MEDTRONIC SOFAMOR DANEK, INC.
X07213190
In Commercial Distribution

  • 00763000595678 ()


  • Surgical retraction system, reusable
BLADE X07213172 LATERAL - L170MM
MEDTRONIC SOFAMOR DANEK, INC.
X07213172
In Commercial Distribution

  • 00763000595661 ()


  • Surgical retraction system, reusable
BLADE X07213171 CRANIAL-CAUDAL L L170MM
MEDTRONIC SOFAMOR DANEK, INC.
X07213171
In Commercial Distribution

  • 00763000595654 ()


  • Surgical retraction system, reusable
BLADE X07213170 CRANIAL-CAUDAL R L170MM
MEDTRONIC SOFAMOR DANEK, INC.
X07213170
In Commercial Distribution

  • 00763000595647 ()


  • Surgical retraction system, reusable
BLADE X07213152 LATERAL - L150MM
MEDTRONIC SOFAMOR DANEK, INC.
X07213152
In Commercial Distribution

  • 00763000595630 ()


  • Surgical retraction system, reusable
BLADE X07213151 CRANIAL-CAUDAL L L150MM
MEDTRONIC SOFAMOR DANEK, INC.
X07213151
In Commercial Distribution

  • 00763000595623 ()


  • Surgical retraction system, reusable
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