PASS LP system

GUDID 03613720271062

TRAY XA02200542 PASS LP ROD TRAY

MEDICREA INTERNATIONAL

Instrument tray, reusable

• Primary Device ID: 03613720271062
• NIH Device Record Key: 5dd0ab39-b1b8-453e-bfd5-70fb7decf45e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PASS LP system
• Version Model Number: XA02200542
• Company DUNS: 383228632
• Company Name: MEDICREA INTERNATIONAL
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	03613720271062 [Primary]

FDA Product Code

• FSM: TRAY, SURGICAL, INSTRUMENT

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-10-09
• Device Publish Date: 2023-09-29

Devices Manufactured by MEDICREA INTERNATIONAL

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• 03613720286677 - IB3D™ PL Spinal System: 2025-03-03 INSERTER A24000000 IB3D IMPLANT
• 03613720286684 - IB3D™ PL Spinal System: 2025-03-03 SLAPHAMMER A24000200 IB3D SLAP HAMMER
• 03613720286707 - IB3D™ PL Spinal System: 2025-03-03 REMOVER A24000220 IB3D IMPLANT REMOVER
• 03613720286202 - IB3D™ PL Spinal System: 2025-02-24 CAGE B241C08062209 3D PL 8X6DGX22X9MM
• 03613720286219 - IB3D™ PL Spinal System: 2025-02-24 CAGE B241C09062209 3D PL 9X6DGX22X9MM
• 03613720286226 - IB3D™ PL Spinal System: 2025-02-24 CAGE B241C10062209 3D PL 10X6DGX22X9MM
• 03613720286233 - IB3D™ PL Spinal System: 2025-02-24 CAGE B241C11062209 3D PL 11X6DGX22X9MM