eudamed_udi Primary ID: 05019829002800

AZOWRAP TRAY LINER 400X500 WHITE (UDI 05019829002800)

Manufactured by Vernacare

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

Scannable UDI-DI Representation

Device Regulatory Overview

The AZOWRAP TRAY LINER 400X500 WHITE (Model/Catalog Number: 92220) is a medical device manufactured by Vernacare. This product is indexed under FDA Product Code / Category Classification S010301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 92220
Product Code / EMDN: S010301
Device Name: Tray Wraps and Tray Liners
Database Sync Date: 2026-08-09 17:43:23

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 AZOWRAP TRAY LINER 400X500 WHITE?

The registered manufacturer of record for AZOWRAP TRAY LINER 400X500 WHITE is Vernacare.

What is the Primary UDI-DI identifier for AZOWRAP TRAY LINER 400X500 WHITE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05019829002800.

What classification code is assigned to this device?

This device is registered under product classification code S010301.

Similar Classification Devices (S010301)

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