GUDIDData
eudamed_udi Primary ID: 08055400675619

VITE A COMPRESSIONE HEADLESS Ø4.0MM L36MM FILETTO COMPLETO ST (UDI 08055400675619)

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 A COMPRESSIONE HEADLESS Ø4.0MM L36MM FILETTO COMPLETO ST - Primary ID 08055400675619

Device Regulatory Overview

The VITE A COMPRESSIONE HEADLESS Ø4.0MM L36MM FILETTO COMPLETO ST (Model/Catalog Number: BSS40036CST) is a medical device manufactured by Mikai s.p.a.. This product is indexed under FDA Product Code / Category Classification P09120603 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
BSS40036CST
Product Code / EMDN
P09120603
Device Name
Headless
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 VITE A COMPRESSIONE HEADLESS Ø4.0MM L36MM FILETTO COMPLETO ST?

The registered manufacturer of record for VITE A COMPRESSIONE HEADLESS Ø4.0MM L36MM FILETTO COMPLETO ST is Mikai s.p.a..

What is the Primary UDI-DI identifier for VITE A COMPRESSIONE HEADLESS Ø4.0MM L36MM FILETTO COMPLETO ST?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08055400675619.

What classification code is assigned to this device?

This device is registered under product classification code P09120603.

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