eudamed_udi Primary ID: 08437012914872

RAÍL ANCLAJE CAMILLA SERIE JÚPITER C-052 (UDI 08437012914872)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The RAÍL ANCLAJE CAMILLA SERIE JÚPITER C-052 (Model/Catalog Number: R-800L52) 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-800L52
Product Code / EMDN: V0805038001
Device Name: RAÍL ANCLAJE CAMILLAS SERIE JÚPITER
Database Sync Date: 2026-08-09 16:58:16

Full Regulatory Attributes

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{
    "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 RAÍL ANCLAJE CAMILLA SERIE JÚPITER C-052?

The registered manufacturer of record for RAÍL ANCLAJE CAMILLA SERIE JÚPITER C-052 is KARTSANA, S.L..

What is the Primary UDI-DI identifier for RAÍL ANCLAJE CAMILLA SERIE JÚPITER C-052?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08437012914872.

What classification code is assigned to this device?

This device is registered under product classification code V0805038001.

Similar Classification Devices (V0805038001)

Other Devices by KARTSANA, S.L.

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