258702000

GUDID 10603295148012

FUKUDA RETRACTOR LARGE

DEPUY (IRELAND)

Hand-held surgical retractor, reusable

• Primary Device ID: 10603295148012
• NIH Device Record Key: 49c13765-cc0a-4c6e-ab7f-ce8bc9333f12
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 2587-02-000
• Catalog Number: 258702000
• Company DUNS: 989365556
• Company Name: DEPUY (IRELAND)
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10603295148012 [Primary]

FDA Product Code

• GAD: RETRACTOR

Sterilization

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

[10603295148012]

Moist Heat or Steam Sterilization

[10603295148012]

Moist Heat or Steam Sterilization

[10603295148012]

Moist Heat or Steam Sterilization

[10603295148012]

Moist Heat or Steam Sterilization

[10603295148012]

Moist Heat or Steam Sterilization

[10603295148012]

Moist Heat or Steam Sterilization

[10603295148012]

Moist Heat or Steam Sterilization

[10603295148012]

Moist Heat or Steam Sterilization

[10603295148012]

Moist Heat or Steam Sterilization

[10603295148012]

Moist Heat or Steam Sterilization

[10603295148012]

Moist Heat or Steam Sterilization

[10603295148012]

Moist Heat or Steam Sterilization

[10603295148012]

Moist Heat or Steam Sterilization

[10603295148012]

Moist Heat or Steam Sterilization

[10603295148012]

Moist Heat or Steam Sterilization

[10603295148012]

Moist Heat or Steam Sterilization

[10603295148012]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-03-26
• Device Publish Date: 2018-09-24

Devices Manufactured by DEPUY (IRELAND)

• 10603295543879 - RECLAIM: 2026-02-02 RECLAIM MONOBLOC REVISION HIP SYSTEM MONOBLOC X-RAY TEMPLATE 115% K
• 10603295543916 - RECLAIM: 2026-02-02 RECLAIM MONOBLOC REVISION HIP SYSTEM MONOBLOC X-RAY TEMPLATE 120% K
• 10603295503309 - ATTUNE: 2026-01-21 Attune Knee System Revision Thick Tibial Base Rotating Platform +10mm Sz 3/1 CEMENTED CAUTION: INTENDED FOR CEMENTED USE ONLY
• 10603295503316 - ATTUNE: 2026-01-21 Attune Knee System Revision Thick Tibial Base Rotating Platform +20mm Sz 3/1 CEMENTED CAUTION: INTENDED FOR CEMENTED USE ONLY
• 10603295503323 - ATTUNE: 2026-01-21 Attune Knee System Revision Thick Tibial Base Rotating Platform +10mm Sz 5/3 CEMENTED CAUTION: INTENDED FOR CEMENTED USE ONLY
• 10603295503330 - ATTUNE: 2026-01-21 Attune Knee System Revision Thick Tibial Base Rotating Platform +20mm Sz 5/2 CEMENTED CAUTION: INTENDED FOR CEMENTED USE ONLY
• 10603295503347 - ATTUNE: 2026-01-21 Attune Knee System Revision Thick Tibial Base Rotating Platform +10mm Sz 7/5 CEMENTED CAUTION: INTENDED FOR CEMENTED USE ONLY
• 10603295503354 - ATTUNE: 2026-01-21 Attune Knee System Revision Thick Tibial Base Rotating Platform +20mm Sz 7/4 CEMENTED CAUTION: INTENDED FOR CEMENTED USE ONLY