AccessGUDID - DEVICE: Discount Drug Mart Food Fair (00093351031854)

GUDID

Device Identifier (DI) Information

Brand Name: Discount Drug Mart Food Fair
Version or Model: 093351031854
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: DISCOUNT DRUG MART, INC.

Primary DI Number: 00093351031854
Issuing Agency: GS1
Commercial Distribution End Date: December 18, 2023
Device Count: 4
Labeler D-U-N-S® Number*: 047741335 *Terms of Use

Device Description: Hydrogel Burn Pads, all one size, 1.96 IN x 2.95 IN (49 mm x 74 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?
47764	Wound hydrogel dressing, non-antimicrobial	A wound covering typically made of cross-linked polymer gels in sheet form or an amorphous hydrating gel of various formulations intended to promote wound healing by maintaining a moist wound environment; it may also facilitate wound debridement and/or absorb exudates in wounds that are minimally to moderately exudative. It may combine hydrogel with supplemental dressing materials (e.g., alginate, film backing), require the use of a secondary dressing, and/or provide a barrier impermeable to liquids and gases; it does not include an antimicrobial agent(s). This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
NAE	Dressing, Wound, Hydrogel Without Drug And/Or Biologic

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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 72ccd7e7-4897-4332-bd47-59d6336f04f5
Public Version Date: November 12, 2024
Public Version Number: 2
DI Record Publish Date: September 14, 2020