AccessGUDID - DEVICE: Kendall (10884527018758)

GUDID

Device Identifier (DI) Information

Brand Name: Kendall
Version or Model: 41550
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 41550
Company Name: Cardinal Health, Inc.

Primary DI Number: 10884527018758
Issuing Agency: GS1
Commercial Distribution End Date: December 31, 2025
Device Count: 2
Labeler D-U-N-S® Number*: 080935429 *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:	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?
34882	Surgical scrub brush, reusable	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 typically consists of a flat handle or a block with side grips on one side, and bristles, fibres, or spines that are typically mounted along a single plane on the other side. This is a reusable 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
Special Storage Condition, Specify: Keep Dry;AVOID DIRECT SUNLIGHT

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 53ce6688-0b4e-4112-830c-732511d0edf5
Public Version Date: June 09, 2023
Public Version Number: 3
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
20884527018755	20	10884527018758	2025-12-31	In Commercial Distribution	CASE

Secondary DI

[?]

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

Unit of Use DI

[?]

Unit of Use DI Number: 30884527018752 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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