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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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Medline Industries, Inc. - 10198459038914

G U MINOR PACK
MEDLINE INDUSTRIES, INC.
DYNJ82737C
In Commercial Distribution

  • 40198459038915 ()
  • 10198459038914 ()
DYNJ82737C

  • General surgical procedure kit, non-medicated, single-use

CARDINAL HEALTH - 10197106922941

R E G PACK
Cardinal Health 200, LLC
SEY41RPA14
In Commercial Distribution

  • 50197106922949 ()
  • 10197106922941 ()
SEY41RPA14

  • Ophthalmic surgical procedure kit, non-medicated, single-use

CARDINAL HEALTH - 10197106557587

KIT, TRIPOINT SHOULDER G
Cardinal Health 200, LLC
PO1DSGLH4
In Commercial Distribution

  • 50197106557585 ()
  • 10197106557587 ()
PO1DSGLH4

  • Orthopaedic surgical procedure kit, medicated

CARDINAL HEALTH - 10197106492468

KIT, TRIPOINT SHOULDER G
Cardinal Health 200, LLC
PO1DSGLHC
In Commercial Distribution

  • 50197106492466 ()
  • 10197106492468 ()
PO1DSGLHC

  • Orthopaedic surgical procedure kit, medicated

CARDINAL HEALTH - 10197106512050

KIT, TRIPOINT SHOULDER G
Cardinal Health 200, LLC
PO1DSGLH3
In Commercial Distribution

  • 50197106512058 ()
  • 10197106512050 ()
PO1DSGLH3

  • Orthopaedic surgical procedure kit, medicated

CARDINAL HEALTH - 10197106511053

R E G PACK
Cardinal Health 200, LLC
SEY41RPA12
In Commercial Distribution

  • 50197106511051 ()
  • 10197106511053 ()
SEY41RPA12

  • Ophthalmic surgical procedure kit, non-medicated, single-use

CARDINAL HEALTH - 10197106506813

KIT, TRIPOINT SHOULDER G
Cardinal Health 200, LLC
PO1DSGLH2
In Commercial Distribution

  • 50197106506811 ()
  • 10197106506813 ()
PO1DSGLH2

  • Orthopaedic surgical procedure kit, medicated

CARDINAL HEALTH - 00887488022300

KIT,G U MAJOR
Cardinal Health 200, LLC
PG5AMJKSJ
In Commercial Distribution

  • 50887488022305 ()
  • 00887488022300 ()
PG5AMJKSJ

  • Urological surgical procedure kit, non-medicated, single-use

ALIF - 00887517640130

ALIF Interfixated Guide, G
Nuvasive, Inc.
1770796
In Commercial Distribution

  • 00887517640130 ()


  • Surgical instrument/implant depth limiter, reusable

BASE - 00887517700278

BASE Guide, Single G
Nuvasive, Inc.
6950107
In Commercial Distribution

  • 00887517700278 ()


  • Surgical instrument/implant depth limiter, reusable
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