eudamed_udi Primary ID: 04026575412020

Unspecified Brand (UDI 04026575412020)

Manufactured by Waldemar Link GmbH & Co. KG

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: 318-215/26) is a medical device manufactured by Waldemar Link GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification P0909030101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 318-215/26
Product Code / EMDN: P0909030101
Device Name: GEMINI SL Total Knee System
Database Sync Date: 2026-08-09 16:44:50

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 Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is Waldemar Link GmbH & Co. KG.

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04026575412020.

What classification code is assigned to this device?

This device is registered under product classification code P0909030101.

Similar Classification Devices (P0909030101)

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