AccessGUDID - DEVICE: Devon (30884527015966)

GUDID

Device Identifier (DI) Information

Brand Name: Devon
Version or Model: 50001501
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 50001501
Company Name: Cardinal Health, Inc.

Primary DI Number: 30884527015966
Issuing Agency: GS1
Commercial Distribution End Date: September 30, 2024
Device Count: 9
Labeler D-U-N-S® Number*: 080935429 *Terms of Use

Device Description: Printed Medication Labels

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?
61575	Skin marking pen, single-use	A dedicated pen intended to be used to delineate areas on the skin surface of a patient (e.g., to outline surgical incision sites, for dermatology applications) utilizing non-toxic ink. It is typically a felt-tip pen which may include a sterile disposable ruler. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FZZ	MARKER, SKIN

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: ;

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 4f29e6f4-71c3-4f97-b176-a0a748a4e271
Public Version Date: September 30, 2024
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
10884527015962	900	30884527015966	2024-09-30	Not in Commercial Distribution	CASE
20884527015969	225	30884527015966	2024-09-30	Not in Commercial Distribution	PACK_OR_INNER_PACK