GUDID 10885074609550

CONSOLE IRC230 LEGEND IRRIGATION EHS EU

MEDTRONIC XOMED, INC.

Surgical power tool system control unit, pneumatic

• Primary Device ID: 10885074609550
• NIH Device Record Key: 15866be2-b6e0-4599-8499-44fb7b922e6a
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: IRC230
• Company DUNS: 835465063
• Company Name: MEDTRONIC XOMED, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: false
• Serial Number: true
• 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	10885074609550 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K012453

FDA Product Code

• HBC: MOTOR, DRILL, ELECTRIC

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2023-11-01
• Device Publish Date: 2016-07-04

Devices Manufactured by MEDTRONIC XOMED, INC.

• 00763000835323 - NIM Neuro: 2025-01-31 MAINFRAME 8253402 NEURO 3.0 INTL EL ROHS
• 00763000835330 - NIM Neuro: 2025-01-31 PATIENT INTFC 8253410 NIM NEURO 3.0 ROHS
• 00763000003036 - NIM Vital™: 2024-11-15 CONN CABLE NIM4CPB2 PAT INTFC NIM 4.0
• 00763000842543 - Bipolar Stimulating Probe: 2024-11-04 PROBE 8225351 5PK CONCEN BIPO STIM ROHS
• 00763000842550 - Bipolar Stimulating Probe: 2024-11-04 PROBE 8225401 5PK SD-SD BIPOL STIM ROHS
• 00763000842567 - Bipolar Stimulating Probe: 2024-11-04 PROBE 8225451 5PK PRASS BIPO STIMUL ROHS
• 00763000891862 - ENT NIM Electrode: 2024-10-01 PROBE 8225275 BALL TIP 1MM ROHS
• 00763000891879 - ENT NIM Electrode: 2024-10-01 PROBE 8225276 BALL TIP 2.3MM ROHS