DURALOC 959986000

GUDID 10603295231899

DURALOC OPTION TRIAL LPW 62 / 64 OR 66 X 28

DEPUY INTERNATIONAL LTD

Acetabulum prosthesis trial, prefabricated, reusable

• Primary Device ID: 10603295231899
• NIH Device Record Key: 522396b0-945b-45d9-a55e-10614c536860
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DURALOC
• Version Model Number: 9599-86-000
• Catalog Number: 959986000
• Company DUNS: 896498813
• Company Name: DEPUY INTERNATIONAL LTD
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10603295231899 [Primary]

FDA Product Code

• HWT: TEMPLATE

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[10603295231899]

Moist Heat or Steam Sterilization

[10603295231899]

Moist Heat or Steam Sterilization

[10603295231899]

Moist Heat or Steam Sterilization

[10603295231899]

Moist Heat or Steam Sterilization

[10603295231899]

Moist Heat or Steam Sterilization

[10603295231899]

Moist Heat or Steam Sterilization

[10603295231899]

Moist Heat or Steam Sterilization

[10603295231899]

Moist Heat or Steam Sterilization

[10603295231899]

Moist Heat or Steam Sterilization

[10603295231899]

Moist Heat or Steam Sterilization

[10603295231899]

Moist Heat or Steam Sterilization

[10603295231899]

Moist Heat or Steam Sterilization

[10603295231899]

Moist Heat or Steam Sterilization

[10603295231899]

Moist Heat or Steam Sterilization

[10603295231899]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-12-21
• Device Publish Date: 2018-09-24

On-Brand Devices [DURALOC]

• 10603295283416: CB DURALOC TRL 10D LINER 64MM
• 10603295283409: CB DURALOC TRL 10D LINER 62MM
• 10603295283362: CB DURALOC TRL 10D LINER 54MM
• 10603295283355: CB DURALOC TRL 10D LINER 52MM
• 10603295283348: CB DURALOC TRL 10D LINER 50MM
• 10603295283331: CB DURALOC TRL 10D LINER 48MM
• 10603295231899: DURALOC OPTION TRIAL LPW 62 / 64 OR 66 X 28
• 10603295231882: DURALOC OPTION TRIAL LPW 58 OR 60 X 28
• 10603295231875: DURALOC OPTION TRIAL LPW 54 OR 56 X 28
• 10603295231868: DURALOC OPTION TRIAL LPW 52 X 28
• 10603295231851: DURALOC OPTION TRIAL LPW 48 OR 50 X 28
• 10603295065685: Duraloc OPTION CUP Enduron Liner LPW 28mmID 62, 64 OR 66mmOD
• 10603295065678: Duraloc OPTION CUP Enduron Liner LPW 28mmID 58 OR 60mmOD
• 10603295065661: Duraloc OPTION CUP Enduron Liner LPW 28mmID 54 OR 56mmOD
• 10603295065654: Duraloc OPTION CUP Enduron Liner LPW 28mmID 52mmOD
• 10603295065647: Duraloc OPTION CUP Enduron Liner LPW 28mmID 48 OR 50mmOD