AccessGUDID - DEVICE: American Red Cross (84617503100018)

GUDID

Device Identifier (DI) Information

Brand Name: American Red Cross
Version or Model: JXB-178
Commercial Distribution Status: In Commercial Distribution
Catalog Number: AR3100
Company Name: CREATIVE CONCEPTS MANUFACTURING LIMITED

Primary DI Number: 84617503100018
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 680004711 *Terms of Use

Device Description: Non-Contact Infrared Thermometer - Quick and Easy Body, Surface and Room Temperature Readings Safe, non-contact thermometer for quick 1 second temperature results in Fahrenheit or Celsius. Multiple operation modes perfect for reading body, room, or surface temperatures with the press of a button. Body mode backlit display illuminates green, yellow or red to clearly indicate normal and elevated temperatures

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?
17888	Infrared patient thermometer, skin	A hand-held, electrically-powered instrument designed to estimate the temperature of a site on the skin (e.g., axilla, forehead) by measurement of body infrared emissions at this particular point. It provides a method to determine temperature patterns or variations on the surface of the skin (e.g., due to differences in perfusion). This device may be used in the home. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FLL	Thermometer, Electronic, Clinical

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: 9f5280f4-9040-4fd1-9029-a0a0f4ffe2d6
Public Version Date: August 02, 2021
Public Version Number: 1
DI Record Publish Date: July 23, 2021