eudamed_udi Primary ID: 08054130002290

Supporto in silicone porta strumenti (UDI 08054130002290)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Supporto in silicone porta strumenti (Model/Catalog Number: S232MIXSTR11) is a medical device manufactured by C.B.M. S.r.l.. This product is indexed under FDA Product Code / Category Classification S0199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: S232MIXSTR11
Product Code / EMDN: S0199
Device Name: Modular system for sterilisation and organisation of surgical instruments
Database Sync Date: 2026-08-09 16:46:23

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 Supporto in silicone porta strumenti?

The registered manufacturer of record for Supporto in silicone porta strumenti is C.B.M. S.r.l..

What is the Primary UDI-DI identifier for Supporto in silicone porta strumenti?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08054130002290.

What classification code is assigned to this device?

This device is registered under product classification code S0199.

Similar Classification Devices (S0199)

Other Devices by C.B.M. S.r.l.

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