AccessGUDID - DEVICE: Nonin Adapter Box Assy for WATCH-PAT 200S-3 (07290109222936)

GUDID

Device Identifier (DI) Information

Brand Name: Nonin Adapter Box Assy for WATCH-PAT 200S-3
Version or Model: Nonin Adapter Box Assy for WATCH-PAT 200S-3
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: US2250306
Company Name: ITAMAR MEDICAL LTD

Primary DI Number: 07290109222936
Issuing Agency: GS1
Commercial Distribution End Date: October 15, 2023
Device Count: 1
Labeler D-U-N-S® Number*: 531857076 *Terms of Use

Device Description: Nonin Adapter Box Assy WatchPAT200 (Recertified)

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?
33843	Polysomnograph	A mains electricity (AC-powered) device designed to record physiological signals from a sleeping patient to assess sleep disorders (e.g., insomnia, snoring or sleep apnoea). The device is typically computerized and usually records an electrocardiogram (ECG), electroencephalogram (EEG), chest wall motion, airflow at both the nose and the mouth, eye movements, haemoglobin oxygen saturation (SpO2) and electromyogram (EMG). Parameters may be added or omitted depending on the study being performed. The device includes multiple electrodes/sensors placed on the patient in specific areas as well as amplifiers and filters for recording.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
MNR	Ventilatory Effort Recorder

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
Storage Environment Temperature: between -20 and 40 Degrees Celsius
Storage Environment Humidity: between 0 and 93 Percent (%) Relative Humidity
Storage Environment Atmospheric Pressure: between 68.95 and 103.42 KiloPascal
Handling Environment Temperature: between 0 and 40 Degrees Celsius
Handling Environment Humidity: between 10 and 93 Percent (%) Relative Humidity
Handling Environment Atmospheric Pressure: between 68.95 and 103.42 KiloPascal

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 21b99ac5-5039-45f3-a438-68b62a73a65b
Public Version Date: October 17, 2023
Public Version Number: 4
DI Record Publish Date: September 07, 2016