GUDIDData
eudamed_udi Primary ID: 05999539855722

TB-F 1R CR Teljes térdízületi protézis femur komponens CR-típus (UDI 05999539855722)

Manufactured by Metrimed Orvosi Műszergyártó Kft.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TB-F 1R CR Teljes térdízületi protézis femur komponens CR-típus - Primary ID 05999539855722

Device Regulatory Overview

The TB-F 1R CR Teljes térdízületi protézis femur komponens CR-típus (Model/Catalog Number: TB-F 1R CR) is a medical device manufactured by Metrimed Orvosi Műszergyártó Kft.. This product is indexed under FDA Product Code / Category Classification P0909030101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
TB-F 1R CR
Product Code / EMDN
P0909030101
Device Name
Total knee joint prosthesis - femoral component
Database Sync Date
2026-08-09 16:28:49

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 TB-F 1R CR Teljes térdízületi protézis femur komponens CR-típus?

The registered manufacturer of record for TB-F 1R CR Teljes térdízületi protézis femur komponens CR-típus is Metrimed Orvosi Műszergyártó Kft..

What is the Primary UDI-DI identifier for TB-F 1R CR Teljes térdízületi protézis femur komponens CR-típus?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05999539855722.

What classification code is assigned to this device?

This device is registered under product classification code P0909030101.

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