GUDIDData
eudamed_udi Primary ID: 05999539856545

VKC 20-40 Spongiosa csavar 6,5 (UDI 05999539856545)

Manufactured by Metrimed Orvosi Műszergyártó Kft.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VKC 20-40 Spongiosa csavar 6,5 - Primary ID 05999539856545

Device Regulatory Overview

The VKC 20-40 Spongiosa csavar 6,5 (Model/Catalog Number: VKC 20-40) is a medical device manufactured by Metrimed Orvosi Műszergyártó Kft.. This product is indexed under FDA Product Code / Category Classification P09088007 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
VKC 20-40
Product Code / EMDN
P09088007
Device Name
Spongiosa screw - for acetabular cage
Database Sync Date
2026-08-09 16:44:57

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 VKC 20-40 Spongiosa csavar 6,5?

The registered manufacturer of record for VKC 20-40 Spongiosa csavar 6,5 is Metrimed Orvosi Műszergyártó Kft..

What is the Primary UDI-DI identifier for VKC 20-40 Spongiosa csavar 6,5?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05999539856545.

What classification code is assigned to this device?

This device is registered under product classification code P09088007.

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