GUDIDData
eudamed_udi Primary ID: D-8680419866613C5

Gold Ortopedi Sanayi ve Ticaret Limited Şirketi (UDI D-8680419866613C5)

Manufactured by GOLD ORTOPEDİ SANAYİ VE TİCARET LİMİTED ŞİRKETİ

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Gold Ortopedi Sanayi ve Ticaret Limited Şirketi - Primary ID D-8680419866613C5

Device Regulatory Overview

The Gold Ortopedi Sanayi ve Ticaret Limited Şirketi (Model/Catalog Number: 70022-06110) is a medical device manufactured by GOLD ORTOPEDİ SANAYİ VE TİCARET LİMİTED ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification P090804010202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
70022-06110
Product Code / EMDN
P090804010202
Device Name
FEMORAL STEM HA COATED - CEMENTLESS 11 mm (Ti)
Database Sync Date
2026-08-09 16:28:45

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 Gold Ortopedi Sanayi ve Ticaret Limited Şirketi?

The registered manufacturer of record for Gold Ortopedi Sanayi ve Ticaret Limited Şirketi is GOLD ORTOPEDİ SANAYİ VE TİCARET LİMİTED ŞİRKETİ.

What is the Primary UDI-DI identifier for Gold Ortopedi Sanayi ve Ticaret Limited Şirketi?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-8680419866613C5.

What classification code is assigned to this device?

This device is registered under product classification code P090804010202.

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