AccessGUDID - DEVICE: Extension cable For TCM3 electrodes, 3m (05700696178537)

GUDID

Device Identifier (DI) Information

Brand Name: Extension cable For TCM3 electrodes, 3m
Version or Model: 617-853
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 617-853
Company Name: Radiometer Medical ApS

Primary DI Number: 05700696178537
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 308667539 *Terms of Use

Device Description: Extension cable For TCM3 electrodes, 3m

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?
47487	Electrical-only medical device connection cable, reusable	A non-patient-contact, insulated, electrical cord with a connector (plug) at both ends designed to transmit electrical power and/or signal (data) between medical devices (e.g., to connect a lead, electrical catheter, handpiece, or monitor to a parent device). It is not intended to connect directly to patient-worn electrodes (i.e., it is not a lead), is not intended to connect to the mains (i.e., not a mains power cable), does not generate any type of power and/or signal, and has no additional non-electrical conducting or processing functionality. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LKD	MONITOR, CARBON-DIOXIDE, CUTANEOUS
LPP	Monitor, oxygen, cutaneous, for uses other than for infant not under gas anesthesia
DQA	Oximeter
KLK	Monitor, oxygen, cutaneous, for infant not under gas anesthesia

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: 86ca15bd-3d57-404e-aef7-1f0f550dd0ca
Public Version Date: August 25, 2023
Public Version Number: 3
DI Record Publish Date: September 01, 2016