GUDIDData
eudamed_udi Primary ID: 08055731434534

VITE CORTICALE AUTOPERFORANTE Ø6MM L150MM F85MM ST (UDI 08055731434534)

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 Ø6MM L150MM F85MM ST - Primary ID 08055731434534

Device Regulatory Overview

The VITE CORTICALE AUTOPERFORANTE Ø6MM L150MM F85MM ST (Model/Catalog Number: VA6.150.85) 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
VA6.150.85
Product Code / EMDN
P09120601
Device Name
Acciaio
Database Sync Date
2026-08-09 16:29:56

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of VITE CORTICALE AUTOPERFORANTE Ø6MM L150MM F85MM ST?

The registered manufacturer of record for VITE CORTICALE AUTOPERFORANTE Ø6MM L150MM F85MM ST is Mikai s.p.a..

What is the Primary UDI-DI identifier for VITE CORTICALE AUTOPERFORANTE Ø6MM L150MM F85MM ST?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08055731434534.

What classification code is assigned to this device?

This device is registered under product classification code P09120601.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint