AccessGUDID - DEVICE: Monoart (E3072171410)

GUDID

Device Identifier (DI) Information

Brand Name: Monoart
Version or Model: Monoart Face Mask Protection 4 Sensitive
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 217141
Company Name: EURONDA SPA

Primary DI Number: E3072171410
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 428755441 *Terms of Use

Device Description: Disposable, hypo-allergenic face mask with 4 layers: a soft water-repellent non-woven fabric for unparalleled protection from dust and moisture; PFE and BFE (Particle Filtration Efficiency and Bacterial Filtration Efficiency) filter; a polymeric filter for excellent fluid resistance, 120 mmHg; a comfortable absorbent hypoallergenic cellulose layer in contact with the skin, for effective absorption of sweat and humidity when used by operators. Built-in nose bridge Made with selected hypo-allergenic materials which have been carefully sourced to respect sensitive skins and avoid the risk of irritation and dermatitis. Box of 50 masks. Colour: Light blue.

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):	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?
66199	Surgical/medical face mask, non-antimicrobial, single-use	A flexible, loose-fitting mask designed to be placed over the mouth and/or nose of a healthcare worker to permit normal breathing while protecting the patient and wearer from the transfer of large particles (e.g., blood, body fluids, and airborne particulate materials). It does not include an antimicrobial/antiviral agent(s) and it is not a form-shaped filtering device (i.e., not a respirator). It is made of a flexible, porous fabric or paper material and is typically secured using elastic head straps or ties; it may incorporate a forming nosepiece (metal wire) and/or transparent face/eye visor. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FXX	Mask, Surgical

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: 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: fcf0e471-4997-49f7-aaa0-0d4bd63b1e66
Public Version Date: April 11, 2025
Public Version Number: 3
DI Record Publish Date: November 29, 2019