Contour 3D™

GUDID 00763000660819

SZR SET 7690S CONTOUR 3D REUSABLE MDR

MEDTRONIC, INC.

Heart valve annulus sizer, reusable

• Primary Device ID: 00763000660819
• NIH Device Record Key: 6fd6ae95-c2a0-46bd-ab24-ccd725c344e8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Contour 3D™
• Version Model Number: 7690S
• Company DUNS: 006261481
• Company Name: MEDTRONIC, 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: false
• 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: false
• 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

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000660819 [Primary]

FDA Product Code

• DTI: SIZER, HEART-VALVE, PROSTHESIS

Sterilization

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

[00763000660819]

Moist Heat or Steam Sterilization

[00763000660819]

Moist Heat or Steam Sterilization

[00763000660819]

Moist Heat or Steam Sterilization

[00763000660819]

Moist Heat or Steam Sterilization

[00763000660819]

Moist Heat or Steam Sterilization

[00763000660819]

Moist Heat or Steam Sterilization

[00763000660819]

Moist Heat or Steam Sterilization

[00763000660819]

Moist Heat or Steam Sterilization

[00763000660819]

Moist Heat or Steam Sterilization

[00763000660819]

Moist Heat or Steam Sterilization

[00763000660819]

Moist Heat or Steam Sterilization

[00763000660819]

Moist Heat or Steam Sterilization

[00763000660819]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-07-28
• Device Publish Date: 2025-07-19

On-Brand Devices [Contour 3D™]

• 00613994845375: RING 690R36 CONTOUR 3D 26L
• 00613994845368: RING 690R34 CONTOUR 3D 26L
• 00613994845351: RING 690R32 CONTOUR 3D 26L
• 00613994845344: RING 690R30 CONTOUR 3D 26L
• 00613994845337: RING 690R28 CONTOUR 3D 26L
• 00613994845320: RING 690R26 CONTOUR 3D 26L
• 00763000660819: SZR SET 7690S CONTOUR 3D REUSABLE MDR
• 00763000660802: RING 690R36 CONTOUR 3D MEX MDR
• 00763000660796: RING 690R34 CONTOUR 3D MEX MDR
• 00763000660789: RING 690R32 CONTOUR 3D MEX MDR
• 00763000660772: RING 690R30 CONTOUR 3D MEX MDR
• 00763000660765: RING 690R28 CONTOUR 3D MEX MDR
• 00763000660758: RING 690R26 CONTOUR 3D MEX MDR