GUDIDData
eudamed_udi Primary ID: 04716770824154

Adult mask (UDI 04716770824154)

Manufactured by Besmed Health Business Corp.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Adult mask - Primary ID 04716770824154

Device Regulatory Overview

The Adult mask (Model/Catalog Number: OM-82415) is a medical device manufactured by Besmed Health Business Corp.. This product is indexed under FDA Product Code / Category Classification R03010302 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
OM-82415
Product Code / EMDN
R03010302
Device Name
MDI Spacer, Silicone mask, 220 ml, adult
Database Sync Date
2026-08-09 17:20:43

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 Adult mask?

The registered manufacturer of record for Adult mask is Besmed Health Business Corp..

What is the Primary UDI-DI identifier for Adult mask?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04716770824154.

What classification code is assigned to this device?

This device is registered under product classification code R03010302.

Programmatic Export

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

JSON API Endpoint