AccessGUDID - DEVICE: AccuTab (00850019755015)

GUDID

Device Identifier (DI) Information

Brand Name: AccuTab
Version or Model: FGN-06-101581
Commercial Distribution Status: In Commercial Distribution
Catalog Number: FGN-06-101581
Company Name: POTRERO MEDICAL, INC.

Primary DI Number: 00850019755015
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 079428290 *Terms of Use

Device Description: AccuTab is a tablet with associated software (AccuData) that connects to the Accuryn Monitor. The tablet is an extension of the Accuryn Monitor and only displays the data that already exists on the Accuryn Monitor. AccuTab with AccuData is solely intended to transfer, store, convert forms, and display medical device data from the Accuryn Monitor.

Device Characteristics

What MRI safety information does the labeling contain?	MR Unsafe
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?
63634	Multi-parameter urinary monitoring system control unit	An electrically-powered component of a multi-parameter urinary monitoring system intended to process and display measurements of urinary output, intra-abdominal pressure (via intra-bladder pressure) and core temperature (via intra-bladder temperature). It is a control unit with a monitor connected to a dedicated disposable catheter set (not included) and is typically used in an intensive care setting to manage acute renal failure. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
OUG	Medical Device Data System

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K221020	000

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: 54cfce24-3106-42a1-a2a0-ae02313e813d
Public Version Date: July 20, 2023
Public Version Number: 2
DI Record Publish Date: April 13, 2023