NA (UDI Table Pad S20CV3)

Manufactured by STERIS

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

Scannable UDI-DI Representation

Device Regulatory Overview

The NA (Model/Catalog Number: Table Pad S20CV3) is a medical device manufactured by STERIS. This product is indexed under FDA Product Code / Category Classification LWG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Table Pad S20CV3
Product Code / EMDN: LWG
Device Name: Cmax Xray 3-inch (80mm) Mattress MFoam Pad is used with the CMAX Xray Surgical Table.
Database Sync Date: 2026-08-09 09:19:08

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 NA?

The registered manufacturer of record for NA is STERIS.

What is the Primary UDI-DI identifier for NA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Table Pad S20CV3.

What classification code is assigned to this device?

This device is registered under product classification code LWG.

Similar Classification Devices (LWG)

Other Devices by STERIS

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