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Monoart

FDA UDI

Class II (US FDA UDI)

by Euronda Spa

Identity

Trade Name
Monoart FDA UDI
Generic Name
Surgical/medical face mask, non-antimicrobial, single-use FDA UDI
Device Name
Disposable, hypo-allergenic face mask with 3 layer: water-repellent non-woven fabric for improved protection against dust and humidity. Box of 50 masks. Carton of 20 boxes. Colour: light blue. FDA UDI
Model / Reference
Monoart Face Mask Protection 3 FDA UDI
Description
Disposable, hypo-allergenic face mask with 3 layer: water-repellent non-woven fabric for improved protection against dust and humidity. Box of 50 masks. Carton of 20 boxes. Colour: light blue. FDA UDI

Identifiers

Catalog Number
217112 FDA UDI
Primary DI / UDI-DI
E3072171120 FDA UDI
FDA Product Code
FXX FDA UDI
GMDN Term
Surgical/medical face mask, non-antimicrobial, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical/medical face mask, non-antimicrobial, single-use

Monoart by Euronda Spa — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/medical face mask, non-antimicrobial, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Euronda Spa

Sources (1)

  • FDA UDI 14b55c51-5f9e-4c44-8c14-aac1390c39c9 34 fields · synced May 30, 2026