Amplatz Goose Neck™

GUDID 00763000762452

SNARE SK201 MICRO SNARE V02

MEDTRONIC, INC.

Intravascular extraction catheter-snare

• Primary Device ID: 00763000762452
• NIH Device Record Key: 96de5b44-7357-4e7e-a356-0e51e99af3ee
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Amplatz Goose Neck™
• Version Model Number: SK201
• Company DUNS: 006261481
• Company Name: MEDTRONIC, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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

Device Dimensions

• Device Size Text, specify: 0
• Catheter Working Length: 175 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Working Length: 175 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Working Length: 175 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Working Length: 175 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Working Length: 175 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Working Length: 175 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Working Length: 175 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Working Length: 175 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Working Length: 175 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Working Length: 175 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Working Length: 175 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Working Length: 175 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Working Length: 175 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Working Length: 175 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Working Length: 175 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Catheter Working Length: 175 Centimeter
• Device Size Text, specify: 0

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep away from sunlight

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000762452 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K970668

FDA Product Code

• DQY: Catheter, percutaneous

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: 2024-11-04
• Device Publish Date: 2024-10-27

On-Brand Devices [Amplatz Goose Neck™]

• 00763000762490: SNARE SK701 MICRO SNARE V02
• 00763000762483: SNARE SK700 MICRO SNARE V02
• 00763000762476: SNARE SK401 MICRO SNARE V02
• 00763000762469: SNARE SK400 MICRO SNARE V02
• 00763000762452: SNARE SK201 MICRO SNARE V02
• 00763000762445: SNARE SK200 MICRO SNARE V02
• 00763000762438: SNARE GN3500 GOOSENECK SNARE V02
• 00763000762421: SNARE GN3000 GOOSENECK SNARE V02
• 00763000762414: SNARE GN2501 GOOSENECK SNARE V02
• 00763000762407: SNARE GN2500 GOOSENECK SNARE V02
• 00763000762391: SNARE GN2000 GOOSENECK SNARE V02
• 00763000762384: SNARE GN1500 GOOSENECK SNARE V02
• 00763000762377: SNARE GN1001 GOOSENECK SNARE V02
• 00763000762360: SNARE GN1000 GOOSENECK SNARE V02
• 00763000762353: SNARE GN500 GOOSENECK SNARE V02