OneView 101247

GUDID 00856298006206

ScottCare’s OneView is an innovative, cardiology software tool used to simplify and streamline the pacemaker/ICD monitoring session reporting process by consolidating all device manufacturers’ session data into one, convenient platform. With a click of a button, OneView captures all relevant pacemaker/ICD data, including:  Device specifications  Measurements for every session  Settings  Episode details  Reports  Physician sign-off OneView also provides insight into historical patient trends and other critical clinical data over time, helping to prioritize patients with more severe issues. In addition, data can be gathered from almost anywhere, as it supports remote interrogation, in-person interrogation and in-person programming.

SCOTTCARE CORPORATION, THE

Cardiology information system application software

• Primary Device ID: 00856298006206
• NIH Device Record Key: 0c938f1f-992c-42b1-99f9-ca16b39fb29f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OneView
• Version Model Number: OneView
• Catalog Number: 101247
• Company DUNS: 808204957
• Company Name: SCOTTCARE CORPORATION, THE
• 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

Customer Support Contacts

• Phone: 216-362-0550
• Email: service@scottcare.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00856298006206 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K061780

FDA Product Code

• DXH: Transmitters And Receivers, Electrocardiograph, Telephone

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: 2016-09-19

Devices Manufactured by SCOTTCARE CORPORATION, THE

• 00856298006428 - EZLink-R: 2024-05-31
• 00856298006435 - EZLink-C: 2024-05-31
• 00856298006008 - Chroma: 2019-11-08 The Chroma model RZ153C Holter monitor is a battery operated solid-state recorder. It is designed for up to 48 hours (2 days) co
• 00856298006015 - Chroma2: 2019-11-08
• 00856298006022 - TeleSenseRCM: 2019-11-08 The TeleSense device is intended for diagnostic evaluation of patients who experience transient symptoms or asymptomatic events
• 00856298006039 - TeleSense-E: 2019-11-08 The TeleSense device is intended for diagnostic evaluation of patients who experience transient symptoms or asymptomatic events
• 00856298006220 - Chroma 5 Lead Patient Cable: 2019-11-08 5 lead ECG patient cable to be used with the Chroma device.
• 00856298006312 - Chroma 7 Lead Patient Cable: 2019-11-08 7 lead ECG patient cable to be used with the Chroma device.