GUDIDData
Bulk Audit Tool API Access
eudamed_udi Primary ID: 08058481760090

MATERASSO ANTIDECUBITO PVC A BOLLE CON RISVOLTI (UDI 08058481760090)

Manufactured by PRAXIS MEDICAL NETWORK SRL

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MATERASSO ANTIDECUBITO PVC A BOLLE CON RISVOLTI - Primary ID 08058481760090

Device Regulatory Overview

The MATERASSO ANTIDECUBITO PVC A BOLLE CON RISVOLTI (Model/Catalog Number: PX16011) is a medical device manufactured by PRAXIS MEDICAL NETWORK SRL. This product is indexed under FDA Product Code / Category Classification V080701 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
PX16011
Product Code / EMDN
V080701
Device Name
AUSILI ANTIDECUBITO
Database Sync Date
2026-08-09 16:29:09

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 MATERASSO ANTIDECUBITO PVC A BOLLE CON RISVOLTI?

The registered manufacturer of record for MATERASSO ANTIDECUBITO PVC A BOLLE CON RISVOLTI is PRAXIS MEDICAL NETWORK SRL.

What is the Primary UDI-DI identifier for MATERASSO ANTIDECUBITO PVC A BOLLE CON RISVOLTI?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08058481760090.

What classification code is assigned to this device?

This device is registered under product classification code V080701.

Similar Classification Devices (V080701)

Other Devices by PRAXIS MEDICAL NETWORK SRL

Programmatic Export

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

JSON API Endpoint