URCHIN™

GUDID 00643169669024

HEART POSITIONER 29700 URCHIN 15L

MEDTRONIC, INC.

Patient positioning vacuum pad

• Primary Device ID: 00643169669024
• NIH Device Record Key: e3a49cc0-f94a-48f8-9109-40e0f4350c56
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: URCHIN™
• Version Model Number: 29700
• 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: 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: 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
• 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	00643169669024 [Primary]

FDA Product Code

• MWS: stabilizer,heart

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-07-08

Devices Manufactured by MEDTRONIC, INC.

• 00613994163516 - Annuloplasty Handle: 2025-12-30 TOOL 7615XL HANDLE ANLO 14L
• 00613994838087 - Contour 3D™: 2025-12-30 TOOL 7690S CNTOUR 3D SZRSET REUSABLE 26L
• 00613994862488 - Annuloplasty Handle: 2025-12-30 TOOL 7686 ANNULOPLASTY HANDLE 216 MM 26L
• 00613994867988 - Medtronic Open Pivot™: 2025-12-30 ACCY 576 MHV SIZER SET
• 00643169525603 - Duran AnCore™: 2025-12-30 SIZER SET 7620S DURAN ANCORE 26L
• 00643169525610 - Annuloplasty Handle: 2025-12-30 HANDLE 7615 ANNULOPLASTY 26L
• 00643169525634 - Annuloplasty Handle: 2025-12-30 HANDLE 7686 ANNULOPLASTY 26L
• 00643169525641 - Annuloplasty Handle: 2025-12-30 HANDLE 7686XL ANNULOPLASTY 26L