AccessGUDID - DEVICE: Urocare® Reusable Latex Leg Bag 44 oz. (00792293095442)

GUDID

Device Identifier (DI) Information

Brand Name: Urocare® Reusable Latex Leg Bag 44 oz.
Version or Model: 9544
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 9544
Company Name: UROCARE PRODUCTS, INC.

Primary DI Number: 00792293095442
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 070637129 *Terms of Use

Device Description: BAG, URINE COLLECTION, LEG, REUSABLE, LATEX, ODOR BARRIER, STRAPS, EXTRA-LARGE, 44 FL. OZ. (1,300 ML.) Contains: Standard Top Adapter #6002, Latex Leg Bag with Odor Barrier, Standard Bottom Drain Valve #6004, Latex Leg Straps with Buttons #6006 and Illustrated Use and Care Instructions.

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):	Yes
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	Yes
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?
58924	Open-ended wearable urine collection bag, non-sterile	A non-sterile flexible plastic pouch designed to connect to a urinary catheter, a urinary condom catheter, or a urostomy bag, and to be strapped to the leg of a patient to collect discharged urine; it is designed with an opening for urine drainage. Also known as a leg bag, it is worn on the body to facilitate patient mobility. This is a single-use device.	Obsolete	false

FDA Product Code

[?]

Product Code	Product Code Name
KNX	Collector, Urine, (And Accessories) For Indwelling Catheter
NNW	Bag, Urine Collection, Leg, For External Use, Non-Sterile

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes 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
Weight: 0.44 Pound
Depth: 1 Inch
Width: 4.75 Inch
Height: 20.625 Inch
Total Volume: 44 Fluid Ounce
Total Volume: 1300 Milliliter

Device Record Status

Public Device Record Key: b6d4a70f-68e5-4f7c-9fc3-3093ce71d843
Public Version Date: July 06, 2018
Public Version Number: 9
DI Record Publish Date: February 05, 2018