eudamed_udi Primary ID: D-8680941263911AH

ZİMED MEDİKAL SAN VE TİCARET LİMİTED ŞİRKETİ (UDI D-8680941263911AH)

Manufactured by Zimed Medikal Sanayi ve Ticaret Limited Şirketi

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

Scannable UDI-DI Representation

Device Regulatory Overview

The ZİMED MEDİKAL SAN VE TİCARET LİMİTED ŞİRKETİ (Model/Catalog Number: E.7503-1002) is a medical device manufactured by Zimed Medikal Sanayi ve Ticaret Limited Şirketi. This product is indexed under FDA Product Code / Category Classification P0909030101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: E.7503-1002
Product Code / EMDN: P0909030101
Device Name: TOTAL KNEE FEMORAL COMPONENT (C/R) CEMENTED 60 MM RIGHT - (CoCr)
Database Sync Date: 2026-08-09 16:28:44

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 ZİMED MEDİKAL SAN VE TİCARET LİMİTED ŞİRKETİ?

The registered manufacturer of record for ZİMED MEDİKAL SAN VE TİCARET LİMİTED ŞİRKETİ is Zimed Medikal Sanayi ve Ticaret Limited Şirketi.

What is the Primary UDI-DI identifier for ZİMED MEDİKAL SAN VE TİCARET LİMİTED ŞİRKETİ?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-8680941263911AH.

What classification code is assigned to this device?

This device is registered under product classification code P0909030101.

Similar Classification Devices (P0909030101)

Other Devices by Zimed Medikal Sanayi ve Ticaret Limited Şirketi

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