AccessGUDID - DEVICE: Kendall (20192253052876)

GUDID

Device Identifier (DI) Information

Brand Name: Kendall
Version or Model: 41550
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 41550
Company Name: Cardinal Health 200, LLC

Primary DI Number: 20192253052876
Issuing Agency: GS1
Commercial Distribution End Date: June 30, 2025
Device Count: 2
Labeler D-U-N-S® Number*: 961027315 *Terms of Use

Device Description: SPONGE STICK WITH PVP-I

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:	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?
47077	Surgical scrub brush, single-use	A hand-held device used by hospital staff to scrub their hands, fingers, and forearms prior to surgery or other intervention where a high degree of personal hygiene is required; it may also be used to mechanically clean the intact skin or superficial wounds of a patient. This device typically has a synthetic sponge surface and a soft bristle surface; it may also include a separate nail cleaner and/or a disinfecting substance. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GEC	BRUSH, SCRUB, OPERATING-ROOM

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 15 and 30 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: d7bc958a-7e09-4f8b-8813-52b741bb0d2f
Public Version Date: June 30, 2025
Public Version Number: 4
DI Record Publish Date: July 29, 2024

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
50192253052877	10	20192253052876	2025-06-30	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: 10192253052879 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: Yes
Manufacturing Date: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

No Customer Contact currently defined

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