AccessGUDID - DEVICE: Clear Image Singles Sterile (30856724004166)

GUDID

Device Identifier (DI) Information

Brand Name: Clear Image Singles Sterile
Version or Model: 04-048-020
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: NEXT MEDICAL PRODUCTS, LLC

Primary DI Number: 30856724004166
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 288
Labeler D-U-N-S® Number*: 078566628 *Terms of Use

Device Description: Clear Image Sterile Ultrasound Gel, 20ml

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:	Yes
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?
58735	Topical coupling gel, sterile	A sterile medium designed to be applied to a patient's skin surface to provide a coupling between an ultrasound transducer and the patient, allowing for the emission and reception of ultrasonic waves that pass through the skin during an ultrasound examination requiring sterile procedure. It is in the form of a non-sticky, drip resistant, fluid-like gel that has been thermally sterilized (contains no degradation products of radiation sterilization) that also assists the operator's ability to move the ultrasound transducer (probe) smoothly over the skin to better scan the site of interest. After application, this device cannot be reused.	Obsolete	false

FDA Product Code

[?]

Product Code	Product Code Name
IYO	System, Imaging, Pulsed Echo, Ultrasonic

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: Yes
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: df299b0f-0c01-4ead-8523-5af61cfa53b1
Public Version Date: June 10, 2022
Public Version Number: 5
DI Record Publish Date: October 24, 2016