Medstorm Defibrillator Pad 16382

GUDID 00863095000108

Medstorm Multi Function Defibrillator Pas, Cardiac Science, Adult, Translucent

BOUND TREE MEDICAL, LLC

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• Primary Device ID: 00863095000108
• NIH Device Record Key: c40ada15-4f50-47d1-9ea6-f1ac59e17bf0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Medstorm Defibrillator Pad
• Version Model Number: T100-CS
• Catalog Number: 16382
• Company DUNS: 070556204
• Company Name: BOUND TREE MEDICAL, LLC
• 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: true
• Manufacturing Date: true
• Expiration Date: true
• 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: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com
• Phone: 614-760-5000
• Email: adam.reuther@sarnova.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00863095000108 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K131494

FDA Product Code

• MKJ: Automated External Defibrillators (Non-Wearable)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2014-11-07

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