GUDIDData
gudid Primary ID: 633049

AtmosAir Velaris (UDI 633049)

Manufactured by Arjohuntleigh AB

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AtmosAir Velaris - Primary ID 633049

Device Regulatory Overview

The AtmosAir Velaris (Model/Catalog Number: 633049) is a medical device manufactured by Arjohuntleigh AB. This product is indexed under FDA Product Code / Category Classification FNM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
633049
Product Code / EMDN
FNM
Device Name
AtmosAir Velaris Mattress - Standard - 810 x 2000 x 180 mm (32 x 79 x 7 in) - Top Cover Premium
Database Sync Date
2026-08-09 09:08:08

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 AtmosAir Velaris?

The registered manufacturer of record for AtmosAir Velaris is Arjohuntleigh AB.

What is the Primary UDI-DI identifier for AtmosAir Velaris?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 633049.

What classification code is assigned to this device?

This device is registered under product classification code FNM.

Programmatic Export

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

JSON API Endpoint