gudid Primary ID: Void OU812a

Filter (UDI Void OU812a)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Filter (Model/Catalog Number: Void OU812a) is a medical device manufactured by WESTMED, INC.. This product is indexed under FDA Product Code / Category Classification CAH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Void OU812a
Product Code / EMDN: CAH
Device Name: Entered in error
Database Sync Date: 2026-08-09 09:04:13

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 Filter?

The registered manufacturer of record for Filter is WESTMED, INC..

What is the Primary UDI-DI identifier for Filter?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Void OU812a.

What classification code is assigned to this device?

This device is registered under product classification code CAH.

Similar Classification Devices (CAH)

Other Devices by WESTMED, INC.

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