AccessGUDID - DEVICE: Bard® Closed System Urinary Drainage Bag (10801741046763)

GUDID

Device Identifier (DI) Information

Brand Name: Bard® Closed System Urinary Drainage Bag
Version or Model: N153504
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: N153504
Company Name: C. R. Bard, Inc.

Primary DI Number: 10801741046763
Issuing Agency: GS1
Commercial Distribution End Date: October 13, 2021
Device Count: 40
Labeler D-U-N-S® Number*: 016898496 *Terms of Use

Device Description: Bard® Closed System Urinary Drainage Bag

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":	Yes
For Single-Use:	Yes
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?
61355	Urethral catheterization support kit, urinary drainage	A collection of non-surgically invasive devices intended to assist a healthcare professional to insert a urethral catheter (not included) into the urinary bladder, typically for drainage of urine; some types may also be intended for catheter removal. It typically includes forceps, dressings, gloves, and drapes; it does not include pharmaceuticals. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
KNX	COLLECTOR, URINE, (AND ACCESSORIES) FOR INDWELLING CATHETER

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
No Device Sizes

Device Record Status

Public Device Record Key: 0cabc04f-a6be-42ea-a069-b141f6fa1cfa
Public Version Date: November 16, 2021
Public Version Number: 5
DI Record Publish Date: August 06, 2016