gudid Primary ID: SML004-PY09

CeroFrict (UDI SML004-PY09)

Manufactured by SML Med-Tech Solutions Limited

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

Scannable UDI-DI Representation

Device Regulatory Overview

The CeroFrict (Model/Catalog Number: SML004-PY09) is a medical device manufactured by SML Med-Tech Solutions Limited. This product is indexed under FDA Product Code / Category Classification CBC within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: SML004-PY09
Product Code / EMDN: CBC
Device Name
Database Sync Date: 2026-08-09 09:46:04

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 CeroFrict?

The registered manufacturer of record for CeroFrict is SML Med-Tech Solutions Limited.

What is the Primary UDI-DI identifier for CeroFrict?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SML004-PY09.

What classification code is assigned to this device?

This device is registered under product classification code CBC.

Similar Classification Devices (CBC)

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