AccessGUDID - DEVICE: Curity (10884521081673)

GUDID

Device Identifier (DI) Information

Brand Name: Curity
Version or Model: 6122
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 6122
Company Name: Cardinal Health, Inc.

Primary DI Number: 10884521081673
Issuing Agency: GS1
Commercial Distribution End Date: September 25, 2021
Device Count: 900
Labeler D-U-N-S® Number*: 080935429 *Terms of Use

Device Description: #10 Burn Dressing,Ready Cut Gauze

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?
61040	Cotton burn dressing, antimicrobial	A covering intended to treat small to large patient burns by being placed over the burn to protect against infection, minimize trauma, skin damage and scarring, and to prevent burn progression. It is made of woven cotton, typically available in various sizes, that is coated with a wound cream which includes both an animal-derived ingredient (e.g., beeswax, animal oil/lard) and an antimicrobial agent (e.g., hepericin). It is typically used by emergency medical services (EMS) and critical care units, but may also be used in the home. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FRL	FIBER, MEDICAL, ABSORBENT

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: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Special Storage Condition, Specify: ;

Clinically Relevant Size

[?]

Size Type Text
Width: 12 Inch
Length: 12 Inch

Device Record Status

Public Device Record Key: ac8fc655-aaa6-4fd2-813a-3b94e7790eae
Public Version Date: October 01, 2025
Public Version Number: 4
DI Record Publish Date: June 30, 2018

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
20884521081670	9000	10884521081673	2021-09-25	Not in Commercial Distribution	CASE

Secondary DI

[?]

Issuing Agency [?]	Secondary DI Number
No Secondary DIs found

Unit of Use DI

[?]

Unit of Use DI Number: 30884521081677 CLOSE

Direct Marking (DM)

[?]

Device Subject to Direct Marking (DM), but Excepted: No
DM DI Different from Primary DI: No
DM DI Number: None
CLOSE

Production Identifier(s) in UDI

[?]

Lot or Batch Number: Yes
Serial Number: No
Expiration Date: No
Manufacturing Date: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

No Customer Contact currently defined

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