Thermasplint

GUDID 20763000040189

SPLINT 1529000 10PK THERMASPLINT SMALL

MEDTRONIC XOMED, INC.

External nasal splint

• Primary Device ID: 20763000040189
• NIH Device Record Key: 08660e29-256d-4e8e-a1ae-d2fe42883737
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Thermasplint
• Version Model Number: 1529000
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000040185 [Primary]
GS1	20763000040189 [Package]; Contains: 00763000040185; Package: PK [10 Units]; In Commercial Distribution

FDA Product Code

• EPP: SPLINT, NASAL

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: 2020-02-24
• Device Publish Date: 2020-02-15

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