GUDID 20763000871837

PATCH AFR-00007 LOCATION REF 4PK US

MEDTRONIC, INC.

Cardiac mapping system reference patch

• Primary Device ID: 20763000871837
• NIH Device Record Key: 3b89bb1c-8734-41a2-b63f-0a68241ee5f7
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: AFR-00007
• 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: true
• 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

Operating and Storage Conditions

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000871833 [Primary]
GS1	20763000871837 [Package]; Contains: 00763000871833; Package: PK [4 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K233943

FDA Product Code

• DQK: Computer, diagnostic, programmable

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-10-29
• Device Publish Date: 2024-10-21

Devices Manufactured by MEDTRONIC, INC.

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• 00763000582906 - Valve Handle 7420: 2025-03-03 HANDLE 7420 VLV HNDLE 234MM CEM GLOBAL
• 00763000911089 - NA: 2025-03-03 FOOT SWITCH NITRONFS GLOBAL
• 20763000954363 - N/A: 2025-03-03 PATCH AFR-00007 LOCATION REF 4PK US
• 20763000999197 - NA: 2025-03-03 CUSTOM PACK BB2N27R2 5PK CARDIO LN
• 20763000999753 - NA: 2025-03-03 CUSTOM PACK 12M79R 10PK TTS
• 20763000999210 - NA: 2025-02-28 CUSTOM PACK BB12D77R2 5PK HEAD PACK
• 20763000999234 - NA: 2025-02-28 CUSTOM PACK BB12D89R1 5PK HEAD ACC PACK