PASS TULIP PRIME

GUDID 03613720293668

HOLDER A22110600 MEDIAL HOOK HOLDER

MEDICREA INTERNATIONAL

Orthopaedic surgical procedure kit, non-medicated, reusable

• Primary Device ID: 03613720293668
• NIH Device Record Key: 909be313-dc56-42f3-9633-9db137a06adb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PASS TULIP PRIME
• Version Model Number: A22110600
• 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	03613720293668 [Primary]

FDA Product Code

• LXH: Orthopedic manual surgical instrument

Sterilization

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

[03613720293668]

Moist Heat or Steam Sterilization

[03613720293668]

Moist Heat or Steam Sterilization

[03613720293668]

Moist Heat or Steam Sterilization

[03613720293668]

Moist Heat or Steam Sterilization

[03613720293668]

Moist Heat or Steam Sterilization

[03613720293668]

Moist Heat or Steam Sterilization

[03613720293668]

Moist Heat or Steam Sterilization

[03613720293668]

Moist Heat or Steam Sterilization

[03613720293668]

Moist Heat or Steam Sterilization

[03613720293668]

Moist Heat or Steam Sterilization

[03613720293668]

Moist Heat or Steam Sterilization

[03613720293668]

Moist Heat or Steam Sterilization

[03613720293668]

Moist Heat or Steam Sterilization

[03613720293668]

Moist Heat or Steam Sterilization

[03613720293668]

Moist Heat or Steam Sterilization

[03613720293668]

Moist Heat or Steam Sterilization

[03613720293668]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-08-05
• Device Publish Date: 2024-07-26

On-Brand Devices [PASS TULIP PRIME]

• 03613720293668: HOLDER A22110600 MEDIAL HOOK HOLDER
• 03613720293651: FORK A22030200 ROCKER FORK
• 03613720293644: DRIVER A22020200 NUT DRIVER