GUDIDData
eudamed_udi Primary ID: 08057502670820

BENDAGGIO PER IMMOBILIZZAZIONE OMERO MIS. XL CM.150X12 (UDI 08057502670820)

Manufactured by DASER S.r.l.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BENDAGGIO PER IMMOBILIZZAZIONE OMERO MIS. XL CM.150X12 - Primary ID 08057502670820

Device Regulatory Overview

The BENDAGGIO PER IMMOBILIZZAZIONE OMERO MIS. XL CM.150X12 (Model/Catalog Number: AS 213.4) is a medical device manufactured by DASER S.r.l.. This product is indexed under FDA Product Code / Category Classification M030501 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
AS 213.4
Product Code / EMDN
M030501
Device Name
Dispositivi per Arto Superiore
Database Sync Date
2026-08-09 16:29:15

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 BENDAGGIO PER IMMOBILIZZAZIONE OMERO MIS. XL CM.150X12?

The registered manufacturer of record for BENDAGGIO PER IMMOBILIZZAZIONE OMERO MIS. XL CM.150X12 is DASER S.r.l..

What is the Primary UDI-DI identifier for BENDAGGIO PER IMMOBILIZZAZIONE OMERO MIS. XL CM.150X12?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08057502670820.

What classification code is assigned to this device?

This device is registered under product classification code M030501.

Programmatic Export

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

JSON API Endpoint