GUDIDData
eudamed_udi Primary ID: 05060131884660

Religrip elasticated tubular bandage size F 10m (UDI 05060131884660)

Manufactured by Reliance Medical Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Religrip elasticated tubular bandage size F 10m - Primary ID 05060131884660

Device Regulatory Overview

The Religrip elasticated tubular bandage size F 10m (Model/Catalog Number: 466) is a medical device manufactured by Reliance Medical Ltd. This product is indexed under FDA Product Code / Category Classification M03030103 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
466
Product Code / EMDN
M03030103
Device Name
Bandage
Database Sync Date
2026-08-09 16:48:27

Full Regulatory Attributes

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

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Frequently Asked Questions

Who is the primary manufacturer of Religrip elasticated tubular bandage size F 10m?

The registered manufacturer of record for Religrip elasticated tubular bandage size F 10m is Reliance Medical Ltd.

What is the Primary UDI-DI identifier for Religrip elasticated tubular bandage size F 10m?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060131884660.

What classification code is assigned to this device?

This device is registered under product classification code M03030103.

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