eudamed_udi Primary ID: 08434048058846

KIT R400+B800+DREPLANC/T (UDI 08434048058846)

Manufactured by PRIM, S.A.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The KIT R400+B800+DREPLANC/T (Model/Catalog Number: KIT-503) is a medical device manufactured by PRIM, S.A.. This product is indexed under FDA Product Code / Category Classification A0699 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: KIT-503
Product Code / EMDN: A0699
Device Name: Agrupaciones de Drenaje
Database Sync Date: 2026-08-09 17:06:04

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 KIT R400+B800+DREPLANC/T?

The registered manufacturer of record for KIT R400+B800+DREPLANC/T is PRIM, S.A..

What is the Primary UDI-DI identifier for KIT R400+B800+DREPLANC/T?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08434048058846.

What classification code is assigned to this device?

This device is registered under product classification code A0699.

Similar Classification Devices (A0699)

Other Devices by PRIM, S.A.

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