AccessGUDID - DEVICE: Cardinal Health™ Surgical Incise Drape with CHG (00817138014973)

GUDID

Device Identifier (DI) Information

Brand Name: Cardinal Health™ Surgical Incise Drape with CHG
Version or Model: 30cm x 35 cm
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 9375
Company Name: AVERY DENNISON CORPORATION

Primary DI Number: 00817138014973
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 40
Labeler D-U-N-S® Number*: 008256364 *Terms of Use

Device Description: Surgical drape containing CHG antimicrobial

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:	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?
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
Special Storage Condition, Specify: No direct sunlight

Clinically Relevant Size

[?]

Size Type Text
Length: 35 Centimeter

Device Record Status

Public Device Record Key: 1f43f395-93e6-4e86-8bf2-90c787b29d61
Public Version Date: June 29, 2023
Public Version Number: 1
DI Record Publish Date: June 21, 2023