GUDIDData
eudamed_udi Primary ID: 08011809021549

GARZE IN COTONE TAGLIATE SENZA FILO RX NON STERILI (UDI 08011809021549)

Manufactured by Santex S.p.A.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GARZE IN COTONE TAGLIATE SENZA FILO RX NON STERILI - Primary ID 08011809021549

Device Regulatory Overview

The GARZE IN COTONE TAGLIATE SENZA FILO RX NON STERILI (Model/Catalog Number: GN3A4040S) is a medical device manufactured by Santex S.p.A.. This product is indexed under FDA Product Code / Category Classification M0201010102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
GN3A4040S
Product Code / EMDN
M0201010102
Device Name
GARZE IN COTONE TAGLIATE SENZA FILO RX NON STERILI
Database Sync Date
2026-08-09 16:46:30

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 GARZE IN COTONE TAGLIATE SENZA FILO RX NON STERILI?

The registered manufacturer of record for GARZE IN COTONE TAGLIATE SENZA FILO RX NON STERILI is Santex S.p.A..

What is the Primary UDI-DI identifier for GARZE IN COTONE TAGLIATE SENZA FILO RX NON STERILI?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08011809021549.

What classification code is assigned to this device?

This device is registered under product classification code M0201010102.

Programmatic Export

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

JSON API Endpoint