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Suction set 2.20 m with terminal cannula Omniasp and autologous bone filterl

FDA UDI

Class I (US FDA UDI)

by Omnia Spa

Identity

Trade Name
Suction set 2.20 m with terminal cannula Omniasp and autologous bone filterl FDA UDI
Generic Name
Dental suction system cannula, single-use FDA UDI
Device Name
Suction set 2.20 m with terminal cannula Omniasp and autologous bone filter FDA UDI
Model / Reference
32.F7077.00 FDA UDI
Description
Suction set 2.20 m with terminal cannula Omniasp and autologous bone filter FDA UDI

Identifiers

Primary DI / UDI-DI
08052141312230 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

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental suction system cannula, single-use

Suction set 2.20 m with terminal cannula Omniasp and autologous bone filterl by Omnia Spa — Class I — FDA UDI — listed in FDA GUDID

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
Omnia Spa

Sources (1)

  • FDA UDI bb7880cf-7023-41f4-9c84-92640711a47d 33 fields · synced Jun 1, 2026