Hancock™ II 7505

GUDID 00763000614034

OBTURATOR 7505SET HK II AORTIC MDR

MEDTRONIC, INC.

Heart valve annulus sizer, reusable

• Primary Device ID: 00763000614034
• NIH Device Record Key: a4d4b80c-e7c8-446c-bf90-28a8e47b5efa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hancock™ II 7505
• Version Model Number: 7505SET
• 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

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 Identifiers

Device Issuing Agency	Device ID
GS1	00763000614034 [Primary]

FDA Product Code

• DTI: SIZER, HEART-VALVE, PROSTHESIS

Sterilization

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

[00763000614034]

Moist Heat or Steam Sterilization

[00763000614034]

Moist Heat or Steam Sterilization

[00763000614034]

Moist Heat or Steam Sterilization

[00763000614034]

Moist Heat or Steam Sterilization

[00763000614034]

Moist Heat or Steam Sterilization

[00763000614034]

Moist Heat or Steam Sterilization

[00763000614034]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-03-11
• Device Publish Date: 2025-03-03

Devices Manufactured by MEDTRONIC, INC.

• 00763000613617 - Mosaic™7308C: 2025-03-11 SIZERS 7308C MOSAIC CINCH AORTIC MDR
• 00763000613624 - Mosaic Ultra™7308U: 2025-03-11 SIZERS 7308U MOSAIC ULTRA AORTIC MDR
• 00763000613631 - Mosaic™7310: 2025-03-11 OBTURATORS 7310 MOSAIC MITRAL MDR
• 00763000613648 - NA: 2025-03-11 HANDLE 7639 VALVE MDR
• 00763000613655 - NA: 2025-03-11 HANDLE 7639XL VALVE XL MDR
• 00763000613662 - NA: 2025-03-11 ACCESSORY 7642 LOCK NUT MDR
• 00763000614034 - Hancock™ II 7505: 2025-03-11OBTURATOR 7505SET HK II AORTIC MDR
• 00763000614034 - Hancock™ II 7505: 2025-03-11 OBTURATOR 7505SET HK II AORTIC MDR
• 00763000614041 - Hancock™ II 7510: 2025-03-11 OBTURATOR 7510SET HK II MITRAL MDR