GUDIDData
eudamed_udi Primary ID: 08051122871759

SECURBIOP MINI 10 - Contenitore da 10 ml preriempito con formaldeide 4% - (UDI 08051122871759)

Manufactured by TRACES S.r.l.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SECURBIOP MINI 10 - Contenitore da 10 ml preriempito con formaldeide 4% - - Primary ID 08051122871759

Device Regulatory Overview

The SECURBIOP MINI 10 - Contenitore da 10 ml preriempito con formaldeide 4% - (Model/Catalog Number: MINI10) is a medical device manufactured by TRACES S.r.l.. This product is indexed under FDA Product Code / Category Classification W050301029099 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
MINI10
Product Code / EMDN
W050301029099
Device Name
Contenitore per campioni bioptici
Database Sync Date
2026-08-09 16:46:37

Full Regulatory Attributes

🔒 Token Gated
{
    "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 SECURBIOP MINI 10 - Contenitore da 10 ml preriempito con formaldeide 4% -?

The registered manufacturer of record for SECURBIOP MINI 10 - Contenitore da 10 ml preriempito con formaldeide 4% - is TRACES S.r.l..

What is the Primary UDI-DI identifier for SECURBIOP MINI 10 - Contenitore da 10 ml preriempito con formaldeide 4% -?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08051122871759.

What classification code is assigned to this device?

This device is registered under product classification code W050301029099.

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