GUDIDData
eudamed_udi Primary ID: 04065803304003

Safestik (UDI 04065803304003)

Manufactured by Geratherm Respiratory GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Safestik - Primary ID 04065803304003

Device Regulatory Overview

The Safestik (Model/Catalog Number: 342200) is a medical device manufactured by Geratherm Respiratory GmbH. This product is indexed under FDA Product Code / Category Classification Z12159080 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
342200
Product Code / EMDN
Z12159080
Device Name
USB-Dongle
Database Sync Date
2026-08-09 17:49:17

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 Safestik?

The registered manufacturer of record for Safestik is Geratherm Respiratory GmbH.

What is the Primary UDI-DI identifier for Safestik?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04065803304003.

What classification code is assigned to this device?

This device is registered under product classification code Z12159080.

Programmatic Export

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

JSON API Endpoint