GUDIDData
eudamed_udi Primary ID: 05944792000082

Sanrotex Medical (UDI 05944792000082)

Manufactured by Bandtex Grup S.R.L.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sanrotex Medical - Primary ID 05944792000082

Device Regulatory Overview

The Sanrotex Medical (Model/Catalog Number: BTX05100) is a medical device manufactured by Bandtex Grup S.R.L.. This product is indexed under FDA Product Code / Category Classification M030101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
BTX05100
Product Code / EMDN
M030101
Device Name
Gauze Bandage
Database Sync Date
2026-08-09 16:29:26

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 Sanrotex Medical?

The registered manufacturer of record for Sanrotex Medical is Bandtex Grup S.R.L..

What is the Primary UDI-DI identifier for Sanrotex Medical?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05944792000082.

What classification code is assigned to this device?

This device is registered under product classification code M030101.

Programmatic Export

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

JSON API Endpoint