AccessGUDID - DEVICE: Basic Adult EPD Femoral Angio Drape (00886333212446)

GUDID

Device Identifier (DI) Information

Brand Name: Basic Adult EPD Femoral Angio Drape
Version or Model: 396111
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 396111
Company Name: ARGON MEDICAL DEVICES, INC.

Primary DI Number: 00886333212446
Issuing Agency: GS1
Commercial Distribution End Date: January 30, 2024
Device Count: 1
Labeler D-U-N-S® Number*: 140727624 *Terms of Use

Device Description: Basic Adult EPD Femoral Angio Drape 75" x 125" w/Full Transparent Windows

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):	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?
47783	Patient surgical drape, single-use	A noninvasive sheet designed to cover a portion of a patient’s anatomy during a surgical procedure to function as a barrier to cross contamination (e.g., isolate a site of surgical incision, protect non-operative anatomy). It is not designed with specific heat-reflective or laser resistant materials. It is available in a variety of designs (e.g., flat sheet with or without an access hole, leg tube or an adhesive film sheet otherwise known as an incise drape). This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
KKX	Drape, Surgical

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
Device Size Text, specify: 75" x 125"

Device Record Status

Public Device Record Key: ab52b1aa-b875-4d44-93ca-6aa8137e4f28
Public Version Date: January 31, 2024
Public Version Number: 3
DI Record Publish Date: September 21, 2016