HeartStart Pads M3718A

GUDID 00884838002876

HeartStart Adult Radiotransparent Pads

Philips Medical Systems

External defibrillator electrode, adult, single-use

• Primary Device ID: 00884838002876
• NIH Device Record Key: 1cee1d1a-a946-426b-b24f-4c14eecb8010
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HeartStart Pads
• Version Model Number: 989803125401
• Catalog Number: M3718A
• Company DUNS: 078628040
• Company Name: Philips Medical Systems
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884838002876 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K002806

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: 2014-09-24

On-Brand Devices [HeartStart Pads]

• 00884838002883: HS Pedi Radiotransparent Pads
• 00884838002876: HeartStart Adult Radiotransparent Pads