GUDIDData
eudamed_udi Primary ID: 08435669508772

AND. AIRON ZERO KIT PISTACHO (UDI 08435669508772)

Manufactured by FABRICACIONES ORTOPEDICAS ALBACETE, S.L.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AND. AIRON ZERO KIT PISTACHO - Primary ID 08435669508772

Device Regulatory Overview

The AND. AIRON ZERO KIT PISTACHO (Model/Catalog Number: 0611.0113) is a medical device manufactured by FABRICACIONES ORTOPEDICAS ALBACETE, S.L.. This product is indexed under FDA Product Code / Category Classification Y120606 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
0611.0113
Product Code / EMDN
Y120606
Device Name
AIRON
Database Sync Date
2026-08-09 16:28:46

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 AND. AIRON ZERO KIT PISTACHO?

The registered manufacturer of record for AND. AIRON ZERO KIT PISTACHO is FABRICACIONES ORTOPEDICAS ALBACETE, S.L..

What is the Primary UDI-DI identifier for AND. AIRON ZERO KIT PISTACHO?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435669508772.

What classification code is assigned to this device?

This device is registered under product classification code Y120606.

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