AccessGUDID - DEVICE: SureStep™ Foley Tray System with Bard® Lubri-Sil® Temp Sensing Foley Catheter (00801741073670)

GUDID

Device Identifier (DI) Information

Brand Name: SureStep™ Foley Tray System with Bard® Lubri-Sil® Temp Sensing Foley Catheter
Version or Model: A119214M
Commercial Distribution Status: In Commercial Distribution
Catalog Number: A119214M
Company Name: C. R. Bard, Inc.

Primary DI Number: 00801741073670
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 016898496 *Terms of Use

Device Description: SureStep® Foley Tray System Lubri-Sil® Temperature Sensing Foley Catheter Tray 350 ml Urine Meter

Device Characteristics

What MRI safety information does the labeling contain?	MR Conditional
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:	Yes
Combination Product:	Yes
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?
32031	Indwelling urethral catheterization kit, adult	A collection of devices that includes an indwelling urethral catheter which incorporates a balloon (commonly known as a Foley catheter), and devices associated with catheter introduction/function (e.g., gloves, lubricating gel, drapes), intended for urinary drainage from the bladder of an adult or paediatric patient. The catheter will be applied by trained staff and may be coated with an antibiotic to help prevent catheter-associated urinary tract infection (CAUTI). This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
EZL	CATHETER, RETENTION TYPE, BALLOON

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
Catheter Gauge: 14 French

Device Record Status

Public Device Record Key: 095c1fdd-d841-49a1-8095-16a5208a2314
Public Version Date: December 04, 2020
Public Version Number: 3
DI Record Publish Date: December 06, 2015