Saver EVO - Saver EVO is a user friendly information - HEARTSINE TECHNOLOGIES LTD

Duns Number:230479318

Device Description: Saver EVO is a user friendly information management program to assist users to manage data Saver EVO is a user friendly information management program to assist users to manage data from their defibrillation device. Saver EVO shall allow the user to download the data from a HeartSine device to a PC computer. Saver EVO™ data management software enables downloading, revie wing and printing ECG waveforms and event history data recorded in HeartSine samaritan PAD devices. Features of Saver EVO include:Comprehensive event documentation to facilitate physician oversight, Utstein style reporting and report export capabilities, User configuration setup and time synchronization, Simple point-and-click operation

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More Product Details

Catalog Number

PAD-ACC-03

Brand Name

Saver EVO

Version/Model Number

1.4.0

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code Details

Product Code

MKJ

Product Code Name

Automated External Defibrillators (Non-Wearable)

Device Record Status

Public Device Record Key

03b8fabc-5c03-4df3-a722-52f4b0fc779f

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

June 10, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"HEARTSINE TECHNOLOGIES LTD" Characteristics
Device Class Device Class Description No of Devices
3 A medical device with high risk that requires premarket approval 28