GUDIDData
eudamed_udi Primary ID: 04250317364302

DG 12,8 D N.3 V=50 STÜ Superior CE (UDI 04250317364302)

Manufactured by Paul Marienfeld GmbH & Co. KG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DG 12,8 D N.3 V=50 STÜ Superior CE - Primary ID 04250317364302

Device Regulatory Overview

The DG 12,8 D N.3 V=50 STÜ Superior CE (Model/Catalog Number: 0114990092) is a medical device manufactured by Paul Marienfeld GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification W0503900202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
0114990092
Product Code / EMDN
W0503900202
Device Name
Microscope slide coverslips (special thickness)
Database Sync Date
2026-08-09 16:28:54

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 DG 12,8 D N.3 V=50 STÜ Superior CE?

The registered manufacturer of record for DG 12,8 D N.3 V=50 STÜ Superior CE is Paul Marienfeld GmbH & Co. KG.

What is the Primary UDI-DI identifier for DG 12,8 D N.3 V=50 STÜ Superior CE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250317364302.

What classification code is assigned to this device?

This device is registered under product classification code W0503900202.

Programmatic Export

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

JSON API Endpoint