Midas Rex Clearview

GUDID 00763000892784

TOOL DC SP14BA30 LGD 14CM PROX 3.0 BALL

MEDTRONIC XOMED, INC.

Orthopaedic bur, reusable

• Primary Device ID: 00763000892784
• NIH Device Record Key: b2b37b51-bde8-41d6-9114-2cd7534447d9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Midas Rex Clearview
• Version Model Number: SP14BA30
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000892784 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K081277

FDA Product Code

• ERL: DRILL, SURGICAL, ENT (ELECTRIC OR PNEUMATIC) INCLUDING HANDPIECE

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-07-01
• Device Publish Date: 2025-06-23

On-Brand Devices [Midas Rex Clearview]

• 00763000892913: TOOL DC SP12MH25 LGD 12CM PROX 2.5 MH
• 00763000892906: TOOL DC SP12MH25T LGD 12CM PROX 2.5 MH3F
• 00763000892890: TOOL DC SP12MH25D LGD 12CM PROX 2.5 MH D
• 00763000892883: TOOL DC SP12MH30 LGD 12CM PROX 3.0 MH
• 00763000892876: TOOL DC SP12MH30D LGD 12CM PROX 3.0 MH D
• 00763000892869: TOOL DC SP12BA30 LGD 12CM PROX 3.0 BALL
• 00763000892852: TOOL DC SP12BA40 LGD 12CM PROX 4.0 BALL
• 00763000892845: TOOL DC SP14MH25 LGD 14CM PROX 2.5 MH
• 00763000892838: TOOL DC SP14MH25T LGD 14CM PROX 2.5 MH3F
• 00763000892821: TOOL DC SP14MH25D LGD 14CM PROX 2.5 MH D
• 00763000892814: TOOL DC SP14MH30 LGD 14CM PROX 3.0 MH
• 00763000892807: TOOL DC SP14MH30T LGD 14CM PROX 3.0 MH3F
• 00763000892791: TOOL DC SP14MH30D LGD 14CM PROX 3.0 MH D
• 00763000892784: TOOL DC SP14BA30 LGD 14CM PROX 3.0 BALL
• 00763000892777: TOOL DC SP14BA40 LGD 14CM PROX 4.0 BALL
• 00763000892760: TOOL DC SD12MH25 LGD 12CM DIST 2.5 MH
• 00763000892753: TOOL DC SD12MH25T LGD 12CM DIST 2.5 MH3F
• 00763000892746: TOOL DC SD12MH25D LGD 12CM DIST 2.5 MH D
• 00763000892739: TOOL DC SD12MH30 LGD 12CM DIST 3.0 MH
• 00763000892722: TOOL DC SD12MH30T LGD 12CM DIST 3.0 MH3F
• 00763000892715: TOOL DC SD12MH30D LGD 12CM DIST 3.0 MH D
• 00763000892708: TOOL DC SD12BA30 LGD 12CM DIST 3.0 BALL
• 00763000892692: TOOL DC SD12BA40 LGD 12CM DIST 4.0 BALL
• 00763000892685: TOOL DC SP12MH30T LGD 12CM PROX 3.0 MH3F