Quadcut®

GUDID 00763000033996

BLADE 1883480HRE QUADCUT 3.4MM X 13CM

MEDTRONIC XOMED, INC.

Oscillating surgical saw blade, single-use

• Primary Device ID: 00763000033996
• NIH Device Record Key: 81f9c53d-3a59-4046-b1b8-2c2057a51e47
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Quadcut®
• Version Model Number: 1883480HRE
• Company DUNS: 835465063
• Company Name: MEDTRONIC XOMED, INC.
• 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: 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
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Dimensions

• Outer Diameter: 3.4 Millimeter
• Outer Diameter: 3.4 Millimeter
• Outer Diameter: 3.4 Millimeter
• Outer Diameter: 3.4 Millimeter
• Outer Diameter: 3.4 Millimeter
• Outer Diameter: 3.4 Millimeter
• Outer Diameter: 3.4 Millimeter
• Outer Diameter: 3.4 Millimeter
• Outer Diameter: 3.4 Millimeter
• Outer Diameter: 3.4 Millimeter
• Outer Diameter: 3.4 Millimeter
• Outer Diameter: 3.4 Millimeter
• Outer Diameter: 3.4 Millimeter
• Outer Diameter: 3.4 Millimeter
• Outer Diameter: 3.4 Millimeter
• Outer Diameter: 3.4 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000033996 [Primary]

FDA Product Code

• EQJ: BUR, EAR, NOSE AND THROAT

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: 2020-03-09
• Device Publish Date: 2020-02-29

On-Brand Devices [Quadcut®]

• 00613994779199: BLADE 1884380HRE QUADCUT 4.3MM X 13CM
• 20613994779186: BLADE 1884380HR QUADCUT 5PK 4.3MM X 13CM
• 00643169101999: BLADE 1883480HRE QUADCUT 3.4MM X 13CM
• 00643169101982: BLADE 1883080HRE QUADCUT 3.0MM X 13CM
• 20763000038162: BLADE 1884380HR QUADCUT 5PK 4.3MM X 13CM
• 00763000033989: BLADE 1883080HRE QUADCUT 3.0MM X 13CM
• 00763000033910: BLADE 1884380HRE QUADCUT 4.3MM X 13CM
• 00763000033996: BLADE 1883480HRE QUADCUT 3.4MM X 13CM