GUDIDData
eudamed_udi Primary ID: 08437021314113

CONJUNTO RAMPA ULTRA-LARGA (UDI 08437021314113)

Manufactured by Productos metálicos del Bages (Promeba)

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CONJUNTO RAMPA ULTRA-LARGA - Primary ID 08437021314113

Device Regulatory Overview

The CONJUNTO RAMPA ULTRA-LARGA (Model/Catalog Number: PB4205-03090) is a medical device manufactured by Productos metálicos del Bages (Promeba). This product is indexed under FDA Product Code / Category Classification V0805038001 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
PB4205-03090
Product Code / EMDN
V0805038001
Device Name
RAÍL
Database Sync Date
2026-08-09 16:47:34

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 CONJUNTO RAMPA ULTRA-LARGA?

The registered manufacturer of record for CONJUNTO RAMPA ULTRA-LARGA is Productos metálicos del Bages (Promeba).

What is the Primary UDI-DI identifier for CONJUNTO RAMPA ULTRA-LARGA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08437021314113.

What classification code is assigned to this device?

This device is registered under product classification code V0805038001.

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