AccessGUDID - DEVICE: Walgreens (00311917192871)

GUDID

Device Identifier (DI) Information

Brand Name: Walgreens
Version or Model: 986721
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: WALGREEN CO.

Primary DI Number: 00311917192871
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 008965063 *Terms of Use

Device Description: Walgreens Stop Lice Complete Treatment Kit (Lice Killing Shampoo, Lice & Egg Combing Spray, Home Spray, and Nit Removal Comb)

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:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	Yes
Kit:	Yes
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?
45370	Lice removal/prevention kit	A collection of non-sterile devices intended to physically and chemically remove human head lice (Pediculus humanus capitis) and/or their eggs (nits) from an infested individual, and/or to prevent (re)infestation. It includes a lice removal and/or prevention agent(s) [e.g., shampoo, solution, emulsion] and also includes additional devices, typically one or more of the following: manual lice comb, shower cap, laundry additive. It does not include lice vacuuming devices. It is normally available [non-prescription] over-the-counter (OTC). This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LJL	Detectors And Removers, Lice, (Including Combs)

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: 21aa967b-6b62-4202-9358-2781cc996797
Public Version Date: December 07, 2020
Public Version Number: 1
DI Record Publish Date: November 27, 2020