GUDIDData
eudamed_udi Primary ID: 08437012914582

RAIL ANCLAJE BRAVO2 DESPLAZAMIENTO LATERAL - LIMA FLUOR (UDI 08437012914582)

Manufactured by KARTSANA, S.L.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RAIL ANCLAJE BRAVO2 DESPLAZAMIENTO LATERAL - LIMA FLUOR - Primary ID 08437012914582

Device Regulatory Overview

The RAIL ANCLAJE BRAVO2 DESPLAZAMIENTO LATERAL - LIMA FLUOR (Model/Catalog Number: R-1002A) is a medical device manufactured by KARTSANA, S.L.. This product is indexed under FDA Product Code / Category Classification V0805038001 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
R-1002A
Product Code / EMDN
V0805038001
Device Name
RAIL ANCLAJE BRAVO2 DESPLAZAMIENTO LATERAL
Database Sync Date
2026-08-09 16:50:49

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of RAIL ANCLAJE BRAVO2 DESPLAZAMIENTO LATERAL - LIMA FLUOR?

The registered manufacturer of record for RAIL ANCLAJE BRAVO2 DESPLAZAMIENTO LATERAL - LIMA FLUOR is KARTSANA, S.L..

What is the Primary UDI-DI identifier for RAIL ANCLAJE BRAVO2 DESPLAZAMIENTO LATERAL - LIMA FLUOR?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08437012914582.

What classification code is assigned to this device?

This device is registered under product classification code V0805038001.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint