GUDIDData
eudamed_udi Primary ID: 04251978600389

Samoa lite Patient Recorder (UDI 04251978600389)

Manufactured by Dr. Fenyves und Gut Deutschland GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Samoa lite Patient Recorder - Primary ID 04251978600389

Device Regulatory Overview

The Samoa lite Patient Recorder (Model/Catalog Number: 929009) is a medical device manufactured by Dr. Fenyves und Gut Deutschland GmbH. This product is indexed under FDA Product Code / Category Classification Z129012 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
929009
Product Code / EMDN
Z129012
Device Name
Polygraphy devices
Database Sync Date
2026-08-09 16:29:32

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 Samoa lite Patient Recorder?

The registered manufacturer of record for Samoa lite Patient Recorder is Dr. Fenyves und Gut Deutschland GmbH.

What is the Primary UDI-DI identifier for Samoa lite Patient Recorder?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251978600389.

What classification code is assigned to this device?

This device is registered under product classification code Z129012.

Programmatic Export

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

JSON API Endpoint