GUDIDData
gudid Primary ID: 110501

AEROBIKA Oscillating Positive Expiratory Pressure Therapy System (UDI 110501)

Manufactured by Trudell Medical International

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AEROBIKA Oscillating Positive Expiratory Pressure Therapy System - Primary ID 110501

Device Regulatory Overview

The AEROBIKA Oscillating Positive Expiratory Pressure Therapy System (Model/Catalog Number: 110501) is a medical device manufactured by Trudell Medical International. This product is indexed under FDA Product Code / Category Classification BWF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
110501
Product Code / EMDN
BWF
Device Name
AEROBIKA Oscillating Positive Expiratory Pressure Therapy System
Database Sync Date
2026-08-09 09:16:47

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 AEROBIKA Oscillating Positive Expiratory Pressure Therapy System?

The registered manufacturer of record for AEROBIKA Oscillating Positive Expiratory Pressure Therapy System is Trudell Medical International.

What is the Primary UDI-DI identifier for AEROBIKA Oscillating Positive Expiratory Pressure Therapy System?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 110501.

What classification code is assigned to this device?

This device is registered under product classification code BWF.

Programmatic Export

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

JSON API Endpoint