gudid Primary ID: 101022

IV-Heart Continuous Nebulizer Pediatric Kit (UDI 101022)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The IV-Heart Continuous Nebulizer Pediatric Kit (Model/Catalog Number: 101022) is a medical device manufactured by WESTMED, INC.. This product is indexed under FDA Product Code / Category Classification CAF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 101022
Product Code / EMDN: CAF
Device Name: IV-Heart Continuous Nebulizer Pediatric Kit
Database Sync Date: 2026-08-09 09:04:13

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of IV-Heart Continuous Nebulizer Pediatric Kit?

The registered manufacturer of record for IV-Heart Continuous Nebulizer Pediatric Kit is WESTMED, INC..

What is the Primary UDI-DI identifier for IV-Heart Continuous Nebulizer Pediatric Kit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 101022.

What classification code is assigned to this device?

This device is registered under product classification code CAF.

Similar Classification Devices (CAF)

Other Devices by WESTMED, INC.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint