GUDIDData
eudamed_udi Primary ID: 08051122871773

SECURBIOP MINI1010 - Contenitore da 10 ml preriempito con formaldeide 8% e 10 ml soluzione fisiologica (UDI 08051122871773)

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 MINI1010 - Contenitore da 10 ml preriempito con formaldeide 8% e 10 ml soluzione fisiologica - Primary ID 08051122871773

Device Regulatory Overview

The SECURBIOP MINI1010 - Contenitore da 10 ml preriempito con formaldeide 8% e 10 ml soluzione fisiologica (Model/Catalog Number: MINI1010FISIO) 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
MINI1010FISIO
Product Code / EMDN
W050301029099
Device Name
Contenitore per campioni bioptici
Database Sync Date
2026-08-09 17:50:41

Full Regulatory Attributes

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

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of SECURBIOP MINI1010 - Contenitore da 10 ml preriempito con formaldeide 8% e 10 ml soluzione fisiologica?

The registered manufacturer of record for SECURBIOP MINI1010 - Contenitore da 10 ml preriempito con formaldeide 8% e 10 ml soluzione fisiologica is TRACES S.r.l..

What is the Primary UDI-DI identifier for SECURBIOP MINI1010 - Contenitore da 10 ml preriempito con formaldeide 8% e 10 ml soluzione fisiologica?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08051122871773.

What classification code is assigned to this device?

This device is registered under product classification code W050301029099.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint