AccessGUDID - DEVICE: MEDRAD® Veris™ 8600 Vital Signs Monitor (00616258009643)

GUDID

Device Identifier (DI) Information

Brand Name: MEDRAD® Veris™ 8600 Vital Signs Monitor
Version or Model: 3010515
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 3010515
Company Name: BAYER MEDICAL CARE INC.

Primary DI Number: 00616258009643
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 058716649 *Terms of Use

Device Description: "PROBE, TEMPERATURE, SKIN (PROBE, TEMPERATURE, SKIN) (85276514)"

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):	Yes
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?
59020	Continuous electronic patient thermometer, line-powered	A mains electricity (AC-powered) electronic instrument designed to continuously measure (monitor) a patient's body temperature (e.g., during the administration of general anaesthesia, treatment of hypothermia and hyperthermia). It comprises an electronic unit and an attached probe that detects and converts the changes in temperature into variations of an electric characteristic, e.g., resistance or voltage. These variations of the electric characteristic are processed in the electronic circuits and continuously displayed as temperature readings. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
MWI	Monitor,Physiological,Patient(Without Arrhythmia Detection Or Alarms)

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K042569	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: 0a539810-0419-46b7-b4e1-9ec3c57189f7
Public Version Date: July 06, 2018
Public Version Number: 2
DI Record Publish Date: April 05, 2018