GUDIDData
eudamed_udi Primary ID: 08436584364504

PEPE - Arnés Grúa de Transferencia (UDI 08436584364504)

Manufactured by Improving Mobility Development SL

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PEPE - Arnés Grúa de Transferencia - Primary ID 08436584364504

Device Regulatory Overview

The PEPE - Arnés Grúa de Transferencia (Model/Catalog Number: P40041) is a medical device manufactured by Improving Mobility Development SL. This product is indexed under FDA Product Code / Category Classification Y183099 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
P40041
Product Code / EMDN
Y183099
Device Name
KMINA and PEPE Home and hygiene assistive products
Database Sync Date
2026-08-09 18:08:38

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 PEPE - Arnés Grúa de Transferencia?

The registered manufacturer of record for PEPE - Arnés Grúa de Transferencia is Improving Mobility Development SL.

What is the Primary UDI-DI identifier for PEPE - Arnés Grúa de Transferencia?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08436584364504.

What classification code is assigned to this device?

This device is registered under product classification code Y183099.

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