GUDIDData
eudamed_udi Primary ID: 08055400670836

VITE CORTICALE AUTOPERFORANTE Ø4MM L200MM F55MM TI ST (UDI 08055400670836)

Manufactured by Mikai s.p.a.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VITE CORTICALE AUTOPERFORANTE Ø4MM L200MM F55MM TI ST - Primary ID 08055400670836

Device Regulatory Overview

The VITE CORTICALE AUTOPERFORANTE Ø4MM L200MM F55MM TI ST (Model/Catalog Number: VA4T200.55) is a medical device manufactured by Mikai s.p.a.. This product is indexed under FDA Product Code / Category Classification P09120601 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
VA4T200.55
Product Code / EMDN
P09120601
Device Name
Titanio
Database Sync Date
2026-08-09 16:30:28

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 VITE CORTICALE AUTOPERFORANTE Ø4MM L200MM F55MM TI ST?

The registered manufacturer of record for VITE CORTICALE AUTOPERFORANTE Ø4MM L200MM F55MM TI ST is Mikai s.p.a..

What is the Primary UDI-DI identifier for VITE CORTICALE AUTOPERFORANTE Ø4MM L200MM F55MM TI ST?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08055400670836.

What classification code is assigned to this device?

This device is registered under product classification code P09120601.

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