StraightShot

GUDID 00763000543815

BLADE 1884002HRE M4 SERR 4MM ROTATE

MEDTRONIC XOMED, INC.

Surgical saw blade, oscillating, single-use

• Primary Device ID: 00763000543815
• NIH Device Record Key: a8c23257-4541-4288-9a02-a2c7626c3e75
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: StraightShot
• Version Model Number: 1884002HRE
• 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: 4 Millimeter
• Length: 11 Centimeter
• Outer Diameter: 4 Millimeter
• Length: 11 Centimeter
• Outer Diameter: 4 Millimeter
• Length: 11 Centimeter
• Outer Diameter: 4 Millimeter
• Length: 11 Centimeter
• Outer Diameter: 4 Millimeter
• Length: 11 Centimeter
• Outer Diameter: 4 Millimeter
• Length: 11 Centimeter
• Outer Diameter: 4 Millimeter
• Length: 11 Centimeter
• Outer Diameter: 4 Millimeter
• Length: 11 Centimeter
• Outer Diameter: 4 Millimeter
• Length: 11 Centimeter
• Outer Diameter: 4 Millimeter
• Length: 11 Centimeter
• Outer Diameter: 4 Millimeter
• Length: 11 Centimeter
• Outer Diameter: 4 Millimeter
• Length: 11 Centimeter
• Outer Diameter: 4 Millimeter
• Length: 11 Centimeter
• Outer Diameter: 4 Millimeter
• Length: 11 Centimeter
• Outer Diameter: 4 Millimeter
• Length: 11 Centimeter
• Outer Diameter: 4 Millimeter
• Length: 11 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000543815 [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: 2021-10-15
• Device Publish Date: 2021-10-07

On-Brand Devices [StraightShot]

• 00763000299286: INSTRUMENT TRAY 1899076 M5
• 00763000299279: INSTRUMENT TRAY 1898075 M4
• 00763000543921: BLADE 1882040HR 5PK M4 INF TURB 2MM ROT
• 00763000543860: BLADE 1882040 5PK INFERIOR TURB 2MM
• 00763000532918: BLADE 1882940HR 5PK M4 INF TURB 2.9MM
• 00763000532857: BLADE 1882940 5PK INFERIOR TURB 2.9MM
• 00763000543815: BLADE 1884002HRE M4 SERR 4MM ROTATE