242033000

GUDID 10603295122616

REV INST STERILIZATION TRAY UPPER

DEPUY ORTHOPAEDICS, INC.

Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable

• Primary Device ID: 10603295122616
• NIH Device Record Key: 33d909ec-e3a0-40dd-9341-525bc30e65f1
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 2420-33-000
• Catalog Number: 242033000
• Company DUNS: 080506581
• Company Name: DEPUY ORTHOPAEDICS, INC.
• 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
• 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	10603295122616 [Primary]

FDA Product Code

• FSM: TRAY, SURGICAL, INSTRUMENT

Sterilization

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

[10603295122616]

Moist Heat or Steam Sterilization

[10603295122616]

Moist Heat or Steam Sterilization

[10603295122616]

Moist Heat or Steam Sterilization

[10603295122616]

Moist Heat or Steam Sterilization

[10603295122616]

Moist Heat or Steam Sterilization

[10603295122616]

Moist Heat or Steam Sterilization

[10603295122616]

Moist Heat or Steam Sterilization

[10603295122616]

Moist Heat or Steam Sterilization

[10603295122616]

Moist Heat or Steam Sterilization

[10603295122616]

Moist Heat or Steam Sterilization

[10603295122616]

Moist Heat or Steam Sterilization

[10603295122616]

Moist Heat or Steam Sterilization

[10603295122616]

Moist Heat or Steam Sterilization

[10603295122616]

Moist Heat or Steam Sterilization

[10603295122616]

Moist Heat or Steam Sterilization

[10603295122616]

Moist Heat or Steam Sterilization

[10603295122616]

Moist Heat or Steam Sterilization

[10603295122616]

Moist Heat or Steam Sterilization

[10603295122616]

Moist Heat or Steam Sterilization

[10603295122616]

Moist Heat or Steam Sterilization

[10603295122616]

Moist Heat or Steam Sterilization

[10603295122616]

Moist Heat or Steam Sterilization

[10603295122616]

Moist Heat or Steam Sterilization

[10603295122616]

Moist Heat or Steam Sterilization

[10603295122616]

Moist Heat or Steam Sterilization

[10603295122616]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2021-07-08
• Device Publish Date: 2018-09-24

Devices Manufactured by DEPUY ORTHOPAEDICS, INC.

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• 10603295123293 - MORELAND: 2024-04-03 MORELAND REV INST TREPHINE REAMER 11mm 5.5 IN
• 10603295123309 - MORELAND: 2024-04-03 MORELAND REV INST TREPHINE REAMER 12.5mm 5.5 IN
• 10603295123316 - MORELAND: 2024-04-03 MORELAND REV INST TREPHINE REAMER 14mm 5.5 IN
• 10603295123323 - MORELAND: 2024-04-03 MORELAND REV INST TREPHINE REAMER 15.5mm 5.5 IN
• 10603295123330 - MORELAND: 2024-04-03 MORELAND REV INST TREPHINE REAMER 17mm 5.5 IN
• 10603295123347 - MORELAND: 2024-04-03 MORELAND REV INST TREPHINE REAMER 18.5mm 5.5 IN
• 10603295123354 - MORELAND: 2024-04-03 MORELAND REV INST TREPHINE REAMER 11mm 9 IN