gudid Primary ID: 22.F6061.00

Sterile Aspiration Tips (UDI 22.F6061.00)

Manufactured by OMNIA SRL

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Sterile Aspiration Tips (Model/Catalog Number: 22.F6061.00) is a medical device manufactured by OMNIA SRL. This product is indexed under FDA Product Code / Category Classification EBR within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 22.F6061.00
Product Code / EMDN: EBR
Device Name: Cannula with ergonomic handle and suction control. (Tip length 15 cm)
Database Sync Date: 2026-08-09 09:04:32

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of Sterile Aspiration Tips?

The registered manufacturer of record for Sterile Aspiration Tips is OMNIA SRL.

What is the Primary UDI-DI identifier for Sterile Aspiration Tips?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 22.F6061.00.

What classification code is assigned to this device?

This device is registered under product classification code EBR.

Similar Classification Devices (EBR)

Other Devices by OMNIA SRL

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