gudid Primary ID: 9409

NeoPod (UDI 9409)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The NeoPod (Model/Catalog Number: 9409) is a medical device manufactured by WESTMED, INC.. This product is indexed under FDA Product Code / Category Classification BTT within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 9409
Product Code / EMDN: BTT
Device Name: Neo-Pod T LavaBed Kit
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 NeoPod?

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

What is the Primary UDI-DI identifier for NeoPod?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9409.

What classification code is assigned to this device?

This device is registered under product classification code BTT.

Similar Classification Devices (BTT)

Other Devices by WESTMED, INC.

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