GUDIDData
eudamed_udi Primary ID: 03760400900931

Mobile Dream standard harnais poignée tournante gauche gris (UDI 03760400900931)

Manufactured by LAZELEC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Mobile Dream standard harnais poignée tournante gauche gris - Primary ID 03760400900931

Device Regulatory Overview

The Mobile Dream standard harnais poignée tournante gauche gris (Model/Catalog Number: Mobile Dream standard harnais poignée tournante gauche gris) is a medical device manufactured by LAZELEC. This product is indexed under FDA Product Code / Category Classification Y122199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
Mobile Dream standard harnais poignée tournante gauche gris
Product Code / EMDN
Y122199
Device Name
Mobile Dream
Database Sync Date
2026-08-09 16:47:14

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 Mobile Dream standard harnais poignée tournante gauche gris?

The registered manufacturer of record for Mobile Dream standard harnais poignée tournante gauche gris is LAZELEC.

What is the Primary UDI-DI identifier for Mobile Dream standard harnais poignée tournante gauche gris?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03760400900931.

What classification code is assigned to this device?

This device is registered under product classification code Y122199.

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