GUDIDData
eudamed_udi Primary ID: 08698454297415

MRG Koşullu HİPOKRAT 2000 Diz Sistemi CR Femur Parçası Sabitleyicili / Çimentolu CoCrMo E.Küçük+ / Sağ (UDI 08698454297415)

Manufactured by HİPOKRAT Tıbbi Malzemeler İmalat ve Pazarlama A.Ş.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MRG Koşullu HİPOKRAT 2000 Diz Sistemi CR Femur Parçası Sabitleyicili / Çimentolu CoCrMo E.Küçük+ / Sağ - Primary ID 08698454297415

Device Regulatory Overview

The MRG Koşullu HİPOKRAT 2000 Diz Sistemi CR Femur Parçası Sabitleyicili / Çimentolu CoCrMo E.Küçük+ / Sağ (Model/Catalog Number: 374.0141) is a medical device manufactured by HİPOKRAT Tıbbi Malzemeler İmalat ve Pazarlama A.Ş.. This product is indexed under FDA Product Code / Category Classification P0909030101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
374.0141
Product Code / EMDN
P0909030101
Device Name
Primer Knee - Fixed Knee Prosthesis System
Database Sync Date
2026-08-09 16:28:46

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 MRG Koşullu HİPOKRAT 2000 Diz Sistemi CR Femur Parçası Sabitleyicili / Çimentolu CoCrMo E.Küçük+ / Sağ?

The registered manufacturer of record for MRG Koşullu HİPOKRAT 2000 Diz Sistemi CR Femur Parçası Sabitleyicili / Çimentolu CoCrMo E.Küçük+ / Sağ is HİPOKRAT Tıbbi Malzemeler İmalat ve Pazarlama A.Ş..

What is the Primary UDI-DI identifier for MRG Koşullu HİPOKRAT 2000 Diz Sistemi CR Femur Parçası Sabitleyicili / Çimentolu CoCrMo E.Küçük+ / Sağ?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08698454297415.

What classification code is assigned to this device?

This device is registered under product classification code P0909030101.

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