H3+ Patient Cable

GUDID 00812345024982

Patient cable cleared with H3+ recorder

MORTARA INSTRUMENT, INC.

Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable

• Primary Device ID: 00812345024982
• NIH Device Record Key: d1a2e5ed-b4d3-4b4e-9b3c-d7bcf223666f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: H3+ Patient Cable
• Version Model Number: 9293-036-51
• 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 Celsius and 65 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 65 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 65 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 65 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00812345024982 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K152626

FDA Product Code

• MWJ: Electrocardiograph,Ambulatory(Without Analysis)

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 [H3+ Patient Cable]

• 00812345025064: Patient cable cleared with H3+ recorder
• 00812345025057: Patient cable cleared with H3+ recorder
• 00812345025040: Patient cable cleared with H3+ recorder
• 00812345025033: Patient cable cleared with H3+ recorder
• 00812345025026: Patient cable cleared with H3+ recorder
• 00812345025002: Patient cable cleared with H3+ recorder
• 00812345024999: Patient cable cleared with H3+ recorder
• 00812345024982: Patient cable cleared with H3+ recorder
• 00812345023084: Patient cable cleared with H3+ recorder
• 00812345023077: Patient cable cleared with H3+ recorder