GUDIDData
gudid Primary ID: UD-46215

Atmos (UDI UD-46215)

Manufactured by DELTA MED SPA

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Atmos - Primary ID UD-46215

Device Regulatory Overview

The Atmos (Model/Catalog Number: UD-46215) is a medical device manufactured by DELTA MED SPA. This product is indexed under FDA Product Code / Category Classification EXQ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
UD-46215
Product Code / EMDN
EXQ
Device Name
Pump Tubing 4x6 mm
Database Sync Date
2026-08-09 09:05:06

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 Atmos?

The registered manufacturer of record for Atmos is DELTA MED SPA.

What is the Primary UDI-DI identifier for Atmos?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is UD-46215.

What classification code is assigned to this device?

This device is registered under product classification code EXQ.

Programmatic Export

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

JSON API Endpoint