GUDIDData
eudamed_udi Primary ID: 05713315009327

Foam Ear Tips (UDI 05713315009327)

Manufactured by Natus Medical Denmark ApS

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Foam Ear Tips - Primary ID 05713315009327

Device Regulatory Overview

The Foam Ear Tips (Model/Catalog Number: 80A4820900) is a medical device manufactured by Natus Medical Denmark ApS. This product is indexed under FDA Product Code / Category Classification Z121401 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
80A4820900
Product Code / EMDN
Z121401
Device Name
Foam Eartip
Database Sync Date
2026-08-09 17:00:02

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 Foam Ear Tips?

The registered manufacturer of record for Foam Ear Tips is Natus Medical Denmark ApS.

What is the Primary UDI-DI identifier for Foam Ear Tips?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05713315009327.

What classification code is assigned to this device?

This device is registered under product classification code Z121401.

Programmatic Export

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

JSON API Endpoint