AccessGUDID - DEVICE: Rite Aid Pharmacy (00011822643146)

GUDID

Device Identifier (DI) Information

Brand Name: Rite Aid Pharmacy
Version or Model: 011822643146
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: RITE AID CORPORATION

Primary DI Number: 00011822643146
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 120
Labeler D-U-N-S® Number*: 014578892 *Terms of Use

Device Description: Advanced antibacterial, Variety Pack Bandages, assorted sizes, Individually boxed, Flexible Fabric: 15- 5/8 IN x 2 1/4 IN (15 mm x 57 mm), 10- 3/4 IN x 3 IN (19 mm x 76 mm); 5- 1 IN x 3 IN (25 mm x 76 mm); Variety Pack: Sport Foam 10- 5/8 IN x 2 1/4 IN ( 15 mm x 57 mm), Watershield Plus 10- 1 IN x 2 1/2 IN ( 25 mm x 63 mm), Strong Strips 10- 1 IN x 3 1/4 IN ( 25 mm x 82 mm); Watershield Plus: 10- 3/4 IN x 2 IN ( 19 mm x 50 mm), 20- 1 IN x 2 1/2 IN ( 25 mm x 63 mm); Flexible Fabric: 10- 1 IN x 3 IN (25 mm x 76 mm); Neon: 20- 3/4 IN x 3 IN (19 mm x 76 mm)

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":	Yes
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?
47378	Skin-cover adhesive strip, antimicrobial	A small, narrow, flexible band (of fabric, plastic, paper, or other material) intended to cover a superficial wound, that is coated on one side with a pressure-sensitive adhesive and that has an absorbent pad prefilled (soaked) with an antiseptic to inhibit the growth of microorganisms. It may also be hypoallergenic and/or waterproof. Commonly referred to as a sticking plaster, it is intended for use in the home or a clinical setting. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
KGX	Tape And Bandage, Adhesive

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No 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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 6505d022-7482-404f-a564-558c5c219384
Public Version Date: June 29, 2021
Public Version Number: 1
DI Record Publish Date: June 21, 2021