GUDIDData
eudamed_udi Primary ID: 04262431121297

RTKS-SET 700g (UDI 04262431121297)

Manufactured by Reintex GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RTKS-SET 700g - Primary ID 04262431121297

Device Regulatory Overview

The RTKS-SET 700g (Model/Catalog Number: RTKS-SET 700g) is a medical device manufactured by Reintex GmbH. This product is indexed under FDA Product Code / Category Classification V08068099 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
RTKS-SET 700g
Product Code / EMDN
V08068099
Device Name
Einweg Patienten-Bettenset
Database Sync Date
2026-08-09 16:28:57

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 RTKS-SET 700g?

The registered manufacturer of record for RTKS-SET 700g is Reintex GmbH.

What is the Primary UDI-DI identifier for RTKS-SET 700g?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04262431121297.

What classification code is assigned to this device?

This device is registered under product classification code V08068099.

Programmatic Export

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

JSON API Endpoint