GUDID 00763000911089

FOOT SWITCH NITRONFS GLOBAL

MEDTRONIC, INC.

Foot-switch, electrical

• Primary Device ID: 00763000911089
• NIH Device Record Key: 2f4a4a2a-a47c-4665-8fbb-f1d0850c68a6
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: NITRONFS
• 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: 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: 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

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000911089 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P020045

FDA Product Code

• LPB: Cardiac ablation percutaneous catheter

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: 2025-03-03
• Device Publish Date: 2025-02-21

Devices Manufactured by MEDTRONIC, INC.

• 00763000582890 - Avalus™ 7400S: 2025-03-03 SIZERS 7400S AVALUS CEM GLOBAL
• 00763000582906 - Valve Handle 7420: 2025-03-03 HANDLE 7420 VLV HNDLE 234MM CEM GLOBAL
• 00763000911089 - NA: 2025-03-03FOOT SWITCH NITRONFS 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