AccessGUDID - DEVICE: PureHorizon (D79010673031)

GUDID

Device Identifier (DI) Information

Brand Name: PureHorizon
Version or Model: 1067303
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 1067303
Company Name: PURELIFE, LLC

Primary DI Number: D79010673031
Issuing Agency: HIBCC
Commercial Distribution End Date: November 15, 2022
Device Count: 200
Labeler D-U-N-S® Number*: 828690904 *Terms of Use

Device Description: Medium, Very soft, stretchy nitrile, Textured fingertips, Blue in color, Packaging contains recycled material

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):	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?
56286	Nitrile examination/treatment glove, non-powdered, non-antimicrobial	A device made of nitrile intended as a protective barrier when worn on the hands of healthcare providers during patient examination/treatment or for other sanitary purposes; its inner surface is not covered with powder and it does not include antimicrobial agents/materials. The device is used mainly as a two-way barrier to protect patient/staff against contaminants and risk of allergy to latex. It will have appropriate characteristics regarding tactility and comfort of use, and should provide appropriate physical properties (e.g., tensile strength, resistance to puncture, elasticity), and uniformity of dimensions (i.e., sizing consistency). This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LZA	Polymer Patient Examination Glove

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K110960	000

Device Exempt from Premarket Submission: No 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: 61263d1b-8ee0-45ac-9a72-4339c49b786c
Public Version Date: November 16, 2022
Public Version Number: 2
DI Record Publish Date: March 26, 2021