AccessGUDID - DEVICE: CARDINAL HEALTH (10885380065415)

GUDID

Device Identifier (DI) Information

Brand Name: CARDINAL HEALTH
Version or Model: BFM68
Commercial Distribution Status: In Commercial Distribution
Catalog Number: BFM68
Company Name: Cardinal Health 200, LLC

Primary DI Number: 10885380065415
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 961027315 *Terms of Use

Device Description: Cardinal Health Silicone Bordered Foam 6 x 8in Dressing Partial to full thickness wounds: -Pressure ulcers -Traumatic wounds (eg. skin tears, road rash and minor injuries) -Diabetic, venous, and arterial ulcers -Graft and donor sites -Post-operative surgical wounds -Lacerations and abrasions Highly absorbent foam pad Gentle silicon adhesive Protective film backing Secure border Directions for use: 1. Clean wound with appropriate wound cleanser such as Cardinal Health Wound Cleanser. Dry surrounding skin thoroughly. Skin barrier products are not necessary. 2. Remove dressing from packaging. For dressings smaller than 5x5 inches, there should be a 3/4-inch overlap onto the dry skin surrounding the wound. For dressings larger than 5x5 inches, there should be a 2-inch overlap. Do not stretch or cut product. 3. Apply adherent side of dressing over wound considering the overlap recommendations to protect the surrounding skin. Secondary dressing or additional fixation is not necessary. 3. All dressings should be monitored frequently. Remove dressing when clinically indicated, such as leakage or increased pain, or after a maximum of 7 days. Not made with natural rubber latex Indications: May be used for the management of moderate to heavy exuding, partial to full thickness wounds, including: -Pressure ulcers -Traumatic wounds (eg. skin tears, road rash and minor injuries) -Diabetic, venous, and arterial ulcers -Graft and donor sites -Post-operative surgical wounds -Lacerations and abrasions

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):	No
Over the Counter (OTC):	Yes
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?
36226	Cavity-wound management dressing, non-antimicrobial	A non-bioabsorbable material or substance designed to be inserted into a wound bed to create an appropriate environment for healing (e.g., warm, moist, absorbent); it does not include an antimicrobial agent(s). It is typically used for the management of deep secondary-healing wounds, particularly for indications such as stage III and IV pressure ulcers, deep leg ulcers, cavity wounds, excisions, and post-op wound dehiscence. It is often designed to conform to the wound bed to support tissues and is often nonadherent to provide for patient comfort during wound management. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
NAD	Dressing, wound, occlusive

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: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Storage Environment Temperature: between 0 and 35 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 0446500f-2bee-492c-8da8-585f61f4f978
Public Version Date: June 19, 2020
Public Version Number: 3
DI Record Publish Date: May 30, 2019