gudid Primary ID: 78404-000

Renalin (UDI 78404-000)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Renalin (Model/Catalog Number: 78404-000) is a medical device manufactured by MEDIVATORS INC.. This product is indexed under FDA Product Code / Category Classification LRJ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 78404-000
Product Code / EMDN: LRJ
Device Name: Renalin
Database Sync Date: 2026-08-09 09:17:21

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 Renalin?

The registered manufacturer of record for Renalin is MEDIVATORS INC..

What is the Primary UDI-DI identifier for Renalin?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 78404-000.

What classification code is assigned to this device?

This device is registered under product classification code LRJ.

Similar Classification Devices (LRJ)

Other Devices by MEDIVATORS INC.

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