GLOBAL APG+ 223000019

GUDID 10603295102922

GLOBAL APG+ BREAKAWAY GUIDE PIN 2.5mm

DEPUY ORTHOPAEDICS, INC.

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Primary Device ID10603295102922
NIH Device Record Keyaf4906a0-5b47-4eb0-90d4-ba09462143e0
Commercial Distribution StatusIn Commercial Distribution
Brand NameGLOBAL APG+
Version Model Number2230-00-019
Catalog Number223000019
Company DUNS080506581
Company NameDEPUY ORTHOPAEDICS, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS110603295102922 [Primary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


[10603295102922]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2022-05-13
Device Publish Date2018-03-15

On-Brand Devices [GLOBAL APG+]

10603295106128GLOBAL APG+ GLENOID IMPACTOR TIP
10603295102946GLOBAL APG+ ANTI-ROTATION PEG INSERTER / REMOVER
10603295105831GLOBAL APG+ PERIPHERAL DRILL GUIDE
10603295105794GLOBAL APG+ ACCESS REAMER SIZE 56
10603295105787GLOBAL APG+ ACCESS REAMER SIZE 52
10603295105770GLOBAL APG+ ACCESS REAMER SIZE 48
10603295105763GLOBAL APG+ ACCESS REAMER SIZE 44
10603295105756GLOBAL APG+ ACCESS REAMER SIZE 40
10603295103097GLOBAL APG+ LOW PROFILE PERIPHERAL REAMER SIZE 56
10603295103080GLOBAL APG+ LOW PROFILE PERIPHERAL REAMER SIZE 52
10603295103073GLOBAL APG+ LOW PROFILE PERIPHERAL REAMER SIZE 48
10603295103066GLOBAL APG+ LOW PROFILE PERIPHERAL REAMER SIZE 44
10603295103059GLOBAL APG+ LOW PROFILE PERIPHERAL REAMER SIZE 40
10603295105961GLOBAL APG+ SIZER PIN GUIDE CADDY +0mm
10603295105916GLOBAL APG+ CASE COMPLETE
10603295105879GLOBAL APG+ TRIAL SIZE 48
10603295105862GLOBAL APG+ TRIAL SIZE 44
10603295105855GLOBAL APG+ TRIAL SIZE 40
10603295105848GLOBAL APG+ GLENOID GRASPER
10603295103455GLOBAL APG+ QUICK CONNECT PERIPHERAL DRILL BIT
10603295102922GLOBAL APG+ BREAKAWAY GUIDE PIN 2.5mm
10603295105909GLOBAL APG+ BONE GRAFT APPLICATOR
10603295105725GLOBAL APG+ SIZER PIN GUIDE SIZE 56 +0mm
10603295105718GLOBAL APG+ SIZER PIN GUIDE SIZE 52 +0mm
10603295105701GLOBAL APG+ SIZER PIN GUIDE SIZE 48 +0mm
10603295105695GLOBAL APG+ SIZER PIN GUIDE SIZE 44 +0mm
10603295105688GLOBAL APG+ SIZER PIN GUIDE SIZE 40 +0mm
10603295103493GLOBAL APG+ ANTI-ROTATION PEG
10603295103028GLOBAL APG+ QUICK CONNECT DRIVER SHAFT
10603295102915GLOBAL APG+ FIXED PIN GUIDE

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