ZOLL CABLE

GUDID 00847946016760

Zoll Medical Corporation

Rechargeable professional automated external defibrillator

• Primary Device ID: 00847946016760
• NIH Device Record Key: b2241636-dc21-4ef9-a0a2-bab806c51b83
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ZOLL CABLE
• Version Model Number: 1009-0913-02
• Company DUNS: 055363428
• Company Name: Zoll Medical Corporation
• 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: false
• OTC Over-The-Counter: false

Operating and Storage Conditions

• Storage Environment Atmospheric Pressure: Between 0 KiloPascal and 0
• Storage Environment Atmospheric Pressure: Between 0 KiloPascal and 0
• Storage Environment Atmospheric Pressure: Between 0 KiloPascal and 0
• Storage Environment Atmospheric Pressure: Between 0 KiloPascal and 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00847946016760 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K120907

FDA Product Code

• LDD: Dc-defibrillator, low-energy, (including paddles)

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: 2014-09-23

On-Brand Devices [ZOLL CABLE]

• 00847946016791: 1007-000505-01
• 00847946016760: 1009-0913-02
• 00847946016753: 1009-0913-01
• 00847946016746: 1009-0918-01
• 00847946016715: 1001-0700
• 00847946016685: 1001-0196-01
• 00847946019891: 1001-001194-01