GUDIDData
eudamed_udi Primary ID: 07395502030635

Unspecified Brand (UDI 07395502030635)

Manufactured by Mediplast AB

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 07395502030635

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: 6050602) is a medical device manufactured by Mediplast AB. This product is indexed under FDA Product Code / Category Classification M0303010101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
6050602
Product Code / EMDN
M0303010101
Device Name
Elastic fixation bandage Danamull
Database Sync Date
2026-08-09 16:58:29

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 Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is Mediplast AB.

What is the Primary UDI-DI identifier for Unspecified Brand?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07395502030635.

What classification code is assigned to this device?

This device is registered under product classification code M0303010101.

Programmatic Export

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

JSON API Endpoint