AccessGUDID - DEVICE: TOSCA 500 Cable (05700699033420)

GUDID

Device Identifier (DI) Information

Brand Name: TOSCA 500 Cable
Version or Model: 903-342
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 903-342
Company Name: Radiometer Basel AG

Primary DI Number: 05700699033420
Issuing Agency: GS1
Commercial Distribution End Date: November 04, 2019
Device Count: 1
Labeler D-U-N-S® Number*: 481337657 *Terms of Use

Device Description: TOSCA 500 Alice DE interface cable. Connecting cable to an external device (PSG).

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?
46934	Transcutaneous blood gas monitoring system	An assembly of mains electricity (AC-powered) devices designed for the continuous and transcutaneous measurement of a patient's blood gas parameters, typically blood partial pressure of oxygen (pO2), blood partial pressure of carbon dioxide (pCO2), haemoglobin oxygen saturation (SpO2), and/or venous blood oxygenation through the jugular vein (SjvO2); often with pulse rate. It consists primarily of a probe for gas detection (e.g., via transcutaneous gas diffusion, or using light spectroscopy) placed on the patient’s skin, and an oximetry monitor for the measurement, analysis, and display of data; patient adhesives and connecting cables may be included.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
DQA	Oximeter
DPZ	Oximeter, ear
LKD	MONITOR, CARBON-DIOXIDE, CUTANEOUS

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: bb921d1f-6159-49d8-ba9c-68765661c8b9
Public Version Date: June 22, 2022
Public Version Number: 3
DI Record Publish Date: September 01, 2016