AccessGUDID - DEVICE: Welch Allyn, Inc. (00732094318432)

GUDID

Device Identifier (DI) Information

Brand Name: Welch Allyn, Inc.
Version or Model: 901007
Commercial Distribution Status: In Commercial Distribution
Catalog Number: QS-6ED-CFEAB
Company Name: WELCH ALLYN, INC.

Primary DI Number: 00732094318432
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 198227881 *Terms of Use

Device Description: Q-Stress Cardiac ver 6 w/ adult & ped interpretation; inc current sfw user manual CD; AM12Q Wired Acquisition Module w/ Trigger Module for TTL/analog signal output;Turnkey system w/ configured CPU & color LCD 24" mon w/ 1920 x 1080 res UK power cord; Z200+ thermal printer,( 2 packs full-grid paper A4), Q-Stress premium cart w/ base, keyboard tray, shelf, large drawer,storage pocket; IEC 10 wire, 12-lead set w/ medi-clips; Iso trans 1000 VA Med Global;Export XML Orders

Device Characteristics

What MRI safety information does the labeling contain?	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):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	Yes
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
35447	Cardiopulmonary stress exercise monitoring system computer	A dedicated computer with a specific software package installed intended to be used to interpret the various physiological parameters and waveforms generated during stress exercise testing of a patient while connected to a stress exercise monitoring system. These signals are provided by appropriate interfaced stress testing devices (e.g., an ergometer) using predefined pattern recognition techniques. The registered signals are compared to pre-established diagnostic criteria.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
DPS	Electrocardiograph

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 5c4da7fb-13b7-4b6b-8461-a59864a2498b
Public Version Date: May 03, 2023
Public Version Number: 1
DI Record Publish Date: April 25, 2023