eudamed_udi Primary ID: 08717371743215

Bandafix (UDI 08717371743215)

Manufactured by Palmedic

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Bandafix (Model/Catalog Number: 916) is a medical device manufactured by Palmedic. This product is indexed under FDA Product Code / Category Classification M03030103 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 916
Product Code / EMDN: M03030103
Device Name: Bandafix
Database Sync Date: 2026-08-09 16:30:39

Full Regulatory Attributes

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{
    "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 Bandafix?

The registered manufacturer of record for Bandafix is Palmedic.

What is the Primary UDI-DI identifier for Bandafix?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08717371743215.

What classification code is assigned to this device?

This device is registered under product classification code M03030103.

Similar Classification Devices (M03030103)

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