Quik-Prep

GUDID 00812345029901

Electrode application system

MORTARA INSTRUMENT, INC.

Electrocardiographic electrode, single-use

• Primary Device ID: 00812345029901
• NIH Device Record Key: 76608927-915b-46ac-b2df-c93c37b07b77
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Quik-Prep
• Version Model Number: 011440-004
• Company DUNS: 062046149
• Company Name: MORTARA INSTRUMENT, 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: 888-667-8272
• Email: techsupport@mortara.com
• Phone: 888-667-8272
• Email: techsupport@mortara.com

Operating and Storage Conditions

• Storage Environment Temperature: Between 0 Degrees Fahrenheit and 185 Degrees Fahrenheit
• Storage Environment Temperature: Between 0 Degrees Fahrenheit and 185 Degrees Fahrenheit

Device Identifiers

Device Issuing Agency	Device ID
GS1	00812345029901 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K782079

FDA Product Code

• DRX: Electrode, Electrocardiograph

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-06-29
• Device Publish Date: 2016-09-24

On-Brand Devices [Quik-Prep]

• 00812345029901: Electrode application system
• 00812345022780: Electrode application system
• 21081234502474: Electrodes
• 21081234502471: Electrodes