GUDIDData
gudid Primary ID: Pony FX

COSMED (UDI Pony FX)

Manufactured by C O S M E D SRL

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for COSMED - Primary ID Pony FX

Device Regulatory Overview

The COSMED (Model/Catalog Number: Pony FX) is a medical device manufactured by C O S M E D SRL. This product is indexed under FDA Product Code / Category Classification DQA within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
Pony FX
Product Code / EMDN
DQA
Device Name
The COSMED Pony FX pulmonary function testing system is a standalone and modular laboratory device for performing the basic lung function tests (Basic Spirometry: Forced Vital Capacity, Slow Vital Capacity, Maximum Voluntary Ventilation) and pulse oximetry.
Database Sync Date
2026-08-09 09:21:50

Full Regulatory Attributes

🔒 Token Gated
{
    "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 COSMED?

The registered manufacturer of record for COSMED is C O S M E D SRL.

What is the Primary UDI-DI identifier for COSMED?

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

What classification code is assigned to this device?

This device is registered under product classification code DQA.

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