gudid Primary ID: Trial Pack

Cerafill RCS (UDI Trial Pack)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Cerafill RCS (Model/Catalog Number: Trial Pack) is a medical device manufactured by PREVEST DENPRO LIMITED. This product is indexed under FDA Product Code / Category Classification KIF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Trial Pack
Product Code / EMDN: KIF
Device Name
Database Sync Date: 2026-08-09 09:01:11

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 Cerafill RCS?

The registered manufacturer of record for Cerafill RCS is PREVEST DENPRO LIMITED.

What is the Primary UDI-DI identifier for Cerafill RCS?

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

What classification code is assigned to this device?

This device is registered under product classification code KIF.

Similar Classification Devices (KIF)

Other Devices by PREVEST DENPRO LIMITED

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