GUDIDData
eudamed_udi Primary ID: 08055731434374

BARRA Ø6MM L150MM ST (UDI 08055731434374)

Manufactured by Mikai s.p.a.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BARRA Ø6MM L150MM ST - Primary ID 08055731434374

Device Regulatory Overview

The BARRA Ø6MM L150MM ST (Model/Catalog Number: 5006.15ST) 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
5006.15ST
Product Code / EMDN
P0912040102
Device Name
ClickIt ER carbon rod
Database Sync Date
2026-08-09 16:44:55

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 BARRA Ø6MM L150MM ST?

The registered manufacturer of record for BARRA Ø6MM L150MM ST is Mikai s.p.a..

What is the Primary UDI-DI identifier for BARRA Ø6MM L150MM ST?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08055731434374.

What classification code is assigned to this device?

This device is registered under product classification code P0912040102.

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