Thermasplint

GUDID 00763000578107

SPLINT 1529020 10PK THERMASPLINT LARGE

MEDTRONIC XOMED, INC.

External nasal splint

• Primary Device ID: 00763000578107
• NIH Device Record Key: 89aec1f7-c598-467b-af53-89e76352f219
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Thermasplint
• Version Model Number: 1529020
• Company DUNS: 835465063
• Company Name: MEDTRONIC XOMED, INC.
• Device Count: 10
• 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
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Dimensions

• Width: 6.7 Centimeter
• Length: 4.4 Centimeter
• Width: 6.7 Centimeter
• Length: 4.4 Centimeter
• Width: 6.7 Centimeter
• Length: 4.4 Centimeter
• Width: 6.7 Centimeter
• Length: 4.4 Centimeter
• Width: 6.7 Centimeter
• Length: 4.4 Centimeter
• Width: 6.7 Centimeter
• Length: 4.4 Centimeter
• Width: 6.7 Centimeter
• Length: 4.4 Centimeter
• Width: 6.7 Centimeter
• Length: 4.4 Centimeter
• Width: 6.7 Centimeter
• Length: 4.4 Centimeter
• Width: 6.7 Centimeter
• Length: 4.4 Centimeter
• Width: 6.7 Centimeter
• Length: 4.4 Centimeter
• Width: 6.7 Centimeter
• Length: 4.4 Centimeter
• Width: 6.7 Centimeter
• Length: 4.4 Centimeter
• Width: 6.7 Centimeter
• Length: 4.4 Centimeter
• Width: 6.7 Centimeter
• Length: 4.4 Centimeter
• Width: 6.7 Centimeter
• Length: 4.4 Centimeter
• Width: 6.7 Centimeter
• Length: 4.4 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000578107 [Unit of Use]
GS1	20763000578101 [Primary]

FDA Product Code

• EPP: SPLINT, NASAL

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-09-24
• Device Publish Date: 2024-09-16

On-Brand Devices [Thermasplint]

• 20763000040189: SPLINT 1529000 10PK THERMASPLINT SMALL
• 20763000040202: SPLINT 1529020 10PK THERMASPLINT LARGE
• 20763000040196: SPLINT 1529010 10PK THERMASPLINT MEDIUM
• 00763000578107: SPLINT 1529020 10PK THERMASPLINT LARGE
• 00763000578091: SPLINT 1529010 10PK THERMASPLINT MEDIUM
• 00763000578084: SPLINT 1529000 10PK THERMASPLINT SMALL