GUDIDData
eudamed_udi Primary ID: 08052990322091

MIR Super SDK Windows (UDI 08052990322091)

Manufactured by MIR - Medical International Research S.p.A.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MIR Super SDK Windows - Primary ID 08052990322091

Device Regulatory Overview

The MIR Super SDK Windows (Model/Catalog Number: 920230) is a medical device manufactured by MIR - Medical International Research S.p.A.. This product is indexed under FDA Product Code / Category Classification Z12150192 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
920230
Product Code / EMDN
Z12150192
Device Name
SSDK
Database Sync Date
2026-08-09 16:50:17

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 MIR Super SDK Windows?

The registered manufacturer of record for MIR Super SDK Windows is MIR - Medical International Research S.p.A..

What is the Primary UDI-DI identifier for MIR Super SDK Windows?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08052990322091.

What classification code is assigned to this device?

This device is registered under product classification code Z12150192.

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