GLOBAL AP 213001120

GUDID 10603295090656

GLOBAL AP HUMERAL HEAD DISTRACTOR

DEPUY (IRELAND)

Orthopaedic implant/instrument dismantling device

• Primary Device ID: 10603295090656
• NIH Device Record Key: 804ceac7-7e7d-4fd1-9659-f2e7de69e11c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GLOBAL AP
• Version Model Number: 2130-01-120
• Catalog Number: 213001120
• 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	10603295090656 [Primary]

FDA Product Code

• HWB: EXTRACTOR

Sterilization

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

[10603295090656]

Moist Heat or Steam Sterilization

[10603295090656]

Moist Heat or Steam Sterilization

[10603295090656]

Moist Heat or Steam Sterilization

[10603295090656]

Moist Heat or Steam Sterilization

[10603295090656]

Moist Heat or Steam Sterilization

[10603295090656]

Moist Heat or Steam Sterilization

[10603295090656]

Moist Heat or Steam Sterilization

[10603295090656]

Moist Heat or Steam Sterilization

[10603295090656]

Moist Heat or Steam Sterilization

[10603295090656]

Moist Heat or Steam Sterilization

[10603295090656]

Moist Heat or Steam Sterilization

[10603295090656]

Moist Heat or Steam Sterilization

[10603295090656]

Moist Heat or Steam Sterilization

[10603295090656]

Moist Heat or Steam Sterilization

[10603295090656]

Moist Heat or Steam Sterilization

[10603295090656]

Moist Heat or Steam Sterilization

[10603295090656]

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: 2018-06-15

Devices Manufactured by DEPUY (IRELAND)

• 10603295085980 - GLOBAL UNITE: 2026-02-09 GLOBAL UNITE COLLAR IMPACTOR
• 10603295088196 - GLOBAL ADVANTAGE: 2026-02-09 GLOBAL ADVANTAGE + IMPACTION BLOCK
• 10603295130192 - ATTUNE: 2026-02-09 ATTUNE TIBIAL IMPACTOR FIXED BEARING
• 10603295130208 - ATTUNE: 2026-02-09 ATTUNE TIBIAL IMPACTOR ROTATING PLATFORM
• 10603295130222 - ATTUNE: 2026-02-09 ATTUNE FEMORAL IMPACTOR
• 10603295395423 - ATTUNE: 2026-02-09 ATTUNE FIXED BEARING INSERT IMPACTOR
• 10603295431275 - DEPUY REACH: 2026-02-09 DEPUY REACH FEMORAL IMPLANT IMPACTOR
• 10603295431596 - DEPUY REACH: 2026-02-09 DEPUY REACH TIBIAL AND INSERT IMPACTOR