GUDIDData
eudamed_udi Primary ID: 08056630552930

SUPPORTO FEMMINA PER VITE/FILO GRANDE M8 A 5 FORI ST (UDI 08056630552930)

Manufactured by Mikai s.p.a.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SUPPORTO FEMMINA PER VITE/FILO GRANDE M8 A 5 FORI ST - Primary ID 08056630552930

Device Regulatory Overview

The SUPPORTO FEMMINA PER VITE/FILO GRANDE M8 A 5 FORI ST (Model/Catalog Number: 5000M92FST) is a medical device manufactured by Mikai s.p.a.. This product is indexed under FDA Product Code / Category Classification P0912040102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
5000M92FST
Product Code / EMDN
P0912040102
Device Name
ClickIt CF
Database Sync Date
2026-08-09 16:30:39

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 SUPPORTO FEMMINA PER VITE/FILO GRANDE M8 A 5 FORI ST?

The registered manufacturer of record for SUPPORTO FEMMINA PER VITE/FILO GRANDE M8 A 5 FORI ST is Mikai s.p.a..

What is the Primary UDI-DI identifier for SUPPORTO FEMMINA PER VITE/FILO GRANDE M8 A 5 FORI ST?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08056630552930.

What classification code is assigned to this device?

This device is registered under product classification code P0912040102.

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