Sterile Aspiration Tips

FDA UDI

Class I (US FDA UDI)

by Omnia Spa

Identity

Trade Name: Sterile Aspiration Tips FDA UDI
Generic Name: Dental suction system cannula, single-use FDA UDI
Device Name: Cannula with ergonomic handle without suction control (Tip length cm 15) FDA UDI
Model / Reference: 22.F6063.00 FDA UDI
Description: Cannula with ergonomic handle without suction control (Tip length cm 15) FDA UDI

Identifiers

Primary DI / UDI-DI: 08052141312636 FDA UDI
FDA Product Code: EBR FDA UDI
GMDN Term: Dental suction system cannula, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.6640 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Dental suction system cannula, single-use

Sterile Aspiration Tips by Omnia Spa — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Omnia Spa

Sources (1)

FDA UDI 6b714c89-f18d-40d6-95e7-993dc9c4a873 33 fields · synced May 30, 2026