AccessGUDID - DEVICE: YASEE (06972359497883)

GUDID

Device Identifier (DI) Information

Brand Name: YASEE
Version or Model: JA-11A
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: QINGDAO YASEE MEDICAL DEVICE CO.,LTD

Primary DI Number: 06972359497883
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 541202125 *Terms of Use

Device Description: Infrared Forehead Thermometer is hand-held, battery powered, Infrared Forehead Thermometers that covert a user’s forehead temperature, using the infrared energy emitted in the area around the user’s forehead to an equivalent temperature when measuring from 1-3 cm of the subject’s forehead with no contact.

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):	No
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?
63711	Infrared patient thermometer, ear/skin	A hand-held, battery-powered, electronic instrument designed to measure: 1) the temperature of a patient's ear canal, typically to estimate the internal (core) temperature; and 2) the temperature of a site on the skin (e.g., axilla, forehead), by measurement of body infrared emissions. It typically includes both a skin-surface tip and an intra-aural tip. This device is intended for use in the home or healthcare facility. 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 [?]
K220084	000

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: 5bdfab02-69db-461d-9155-2a0011502e74
Public Version Date: December 06, 2023
Public Version Number: 1
DI Record Publish Date: November 28, 2023