AccessGUDID - DEVICE: Scanlan® PrepMARK (00846159025392)

GUDID

Device Identifier (DI) Information

Brand Name: Scanlan® PrepMARK
Version or Model: 1001-731
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 1001-731
Company Name: SCANLAN INTERNATIONAL INC

Primary DI Number: 00846159025392
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 023055619 *Terms of Use

Device Description: Scanlan® PrepMARK - Reg Tip, Gentian Violet, Non-Sterile, Box 50

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):	Yes
Over the Counter (OTC):	No
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?
61576	Skin marking pen, single-use, non-sterile	A non-sterile, dedicated pen (typically a felt-tip pen) intended to be used to delineate areas on the skin surface of a patient (e.g., for dermatology applications) utilizing non-toxic ink. This is a single-use device.	Obsolete	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: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 4f6e4eee-0b48-4c5d-a563-a91d016548be
Public Version Date: January 14, 2019
Public Version Number: 1
DI Record Publish Date: December 12, 2018