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Monoart

FDA UDI

Class I (US FDA UDI)

by Euronda Spa

Identity

Trade Name
Monoart FDA UDI
Generic Name
Dental suction system cannula, single-use FDA UDI
Device Name
Practical kit Monoart containing 5 different disposable products for 500 patients: 500 Towel Up, 500 saliva ejectors fix, 500 plastic cups, 200 Masks Pro.3, 160 Aprons PG30/80. Colour: light blue FDA UDI
Model / Reference
KIT MONOART® 5P 15,0 FIXED FDA UDI
Description
Practical kit Monoart containing 5 different disposable products for 500 patients: 500 Towel Up, 500 saliva ejectors fix, 500 plastic cups, 200 Masks Pro.3, 160 Aprons PG30/80. Colour: light blue FDA UDI

Identifiers

Catalog Number
290202 FDA UDI
Primary DI / UDI-DI
E3072902021 FDA UDI
FDA Product Code
KHR FDA UDI
GMDN Term
Dental suction system cannula, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6050 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

Yes

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, single-useDental suction system cannula, single-use

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

Similar devices

Also classified as Dental suction system cannula, 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 d5f83eec-3833-4a3f-9bfc-959b5da53cdd 34 fields · synced Jun 1, 2026