Welch Allyn, Inc. - HScribe Holter Analysis System - version 6 with - WELCH ALLYN, INC.

Duns Number:198227881

Device Description: HScribe Holter Analysis System - version 6 with adult and pediatric arrhythmia analysis. HScribe Holter Analysis System - version 6 with adult and pediatric arrhythmia analysis. Includes current software CD, user manual CD, CF card reader, and H3+ USB interface cable; Standard model; Software kit; Australia power cord; No printer; Rx Report Export (UNIPRO and waveform XML) + DICOM bidirectional Interface

Want to know more about this Product? Request more information now!


More Product Details

Catalog Number

HSCRIBE-6AC-BXXXE

Brand Name

Welch Allyn, Inc.

Version/Model Number

901143

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)

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

MLO

Product Code Name

ELECTROCARDIOGRAPH, AMBULATORY, WITH ANALYSIS ALGORITHM

Device Record Status

Public Device Record Key

37e782e6-6063-48cd-b6fe-d69524d7ad6b

Public Version Date

June 28, 2022

Public Version Number

2

DI Record Publish Date

September 25, 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