Tubing

GUDID 00847946021702

DUAL LUMEN NIBP TUBING ASSEMBLY

Zoll Medical Corporation

Rechargeable professional automated external defibrillator

• Primary Device ID: 00847946021702
• NIH Device Record Key: 02615b3f-2894-4692-8ab3-da6d44ff3971
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tubing
• Version Model Number: 3007-0002
• Company DUNS: 055363428
• Company Name: Zoll Medical Corporation
• Device Count: 1
• DM Exempt: true
• 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: false
• 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 Humidity: Between 0 Percent (%) Relative Humidity and 0 Percent (%) Relative Humidity
• Storage Environment Humidity: Between 0 Percent (%) Relative Humidity and 0 Percent (%) Relative Humidity
• Storage Environment Humidity: Between 0 Percent (%) Relative Humidity and 0 Percent (%) Relative Humidity
• Storage Environment Humidity: Between 0 Percent (%) Relative Humidity and 0 Percent (%) Relative Humidity

Device Identifiers

Device Issuing Agency	Device ID
GS1	00847946021702 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K142915

FDA Product Code

• DXN: SYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE

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: 2016-09-16

On-Brand Devices [Tubing]

• 00847946021719: DUAL LUMEN NIBP TUBING ASSEMBLY, 5 FT
• 00847946021702: DUAL LUMEN NIBP TUBING ASSEMBLY