Welch Allyn, Inc. - ELI280 12-Lead Multi-Channel Electrocardiograph - - WELCH ALLYN, INC.

Duns Number:198227881

Device Description: ELI280 12-Lead Multi-Channel Electrocardiograph - Resistive color touchscreen 10.1" displa ELI280 12-Lead Multi-Channel Electrocardiograph - Resistive color touchscreen 10.1" display, AC or battery operation with WAM Wireless Acquisition Module (includes 1 starter pack paper - A4 with spacer for writer tray); current software; US/Canada power cord; IEC 10 wire, 12- lead lead set with banana plugs; Adult and pediatric interpretation; No accessories; Ethernet LAN + USBD; Standard storage (up to 40 ECGs);DICOM (Bidirectional communication with third party data management system)

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More Product Details

Catalog Number

ELI280-DAB-ADCAD

Brand Name

Welch Allyn, Inc.

Version/Model Number

901132

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code Details

Product Code

DPS

Product Code Name

Electrocardiograph

Device Record Status

Public Device Record Key

43eba576-c69d-4294-9d06-e4cd4239b84f

Public Version Date

June 29, 2022

Public Version Number

3

DI Record Publish Date

July 01, 2019

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"WELCH ALLYN, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 374
2 A medical device with a moderate to high risk that requires special controls. 4080
3 A medical device with high risk that requires premarket approval 1