GUDIDData
eudamed_udi Primary ID: 08055731435937

VITE CORTICALE AUTOPERFORANTE Ø2MM L40MM F10MM TI ST (UDI 08055731435937)

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 Ø2MM L40MM F10MM TI ST - Primary ID 08055731435937

Device Regulatory Overview

The VITE CORTICALE AUTOPERFORANTE Ø2MM L40MM F10MM TI ST (Model/Catalog Number: 5002422TST) 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
5002422TST
Product Code / EMDN
P09120601
Device Name
Titanio
Database Sync Date
2026-08-09 16:29:29

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 Ø2MM L40MM F10MM TI ST?

The registered manufacturer of record for VITE CORTICALE AUTOPERFORANTE Ø2MM L40MM F10MM TI ST is Mikai s.p.a..

What is the Primary UDI-DI identifier for VITE CORTICALE AUTOPERFORANTE Ø2MM L40MM F10MM TI ST?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08055731435937.

What classification code is assigned to this device?

This device is registered under product classification code P09120601.

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