GUDIDData
eudamed_udi Primary ID: 04251816802166

UUS-3058/E (UDI 04251816802166)

Manufactured by AGA Sanitätsartikel GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for UUS-3058/E - Primary ID 04251816802166

Device Regulatory Overview

The UUS-3058/E (Model/Catalog Number: 78) is a medical device manufactured by AGA Sanitätsartikel GmbH. This product is indexed under FDA Product Code / Category Classification V08020199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
78
Product Code / EMDN
V08020199
Device Name
Untersuchungsstuhl
Database Sync Date
2026-08-09 16:28:49

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 UUS-3058/E?

The registered manufacturer of record for UUS-3058/E is AGA Sanitätsartikel GmbH.

What is the Primary UDI-DI identifier for UUS-3058/E?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251816802166.

What classification code is assigned to this device?

This device is registered under product classification code V08020199.

Programmatic Export

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

JSON API Endpoint