GUDIDData
eudamed_udi Primary ID: EWWV182300031

Curadent Zellstofftupfer 4 x 5 cm (UDI EWWV182300031)

Manufactured by Wilhelm Weisweiler GmbH & Co. KG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Curadent Zellstofftupfer 4 x 5 cm - Primary ID EWWV182300031

Device Regulatory Overview

The Curadent Zellstofftupfer 4 x 5 cm (Model/Catalog Number: 18230003) is a medical device manufactured by Wilhelm Weisweiler GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification M0199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
18230003
Product Code / EMDN
M0199
Device Name
Zellstofftupfer
Database Sync Date
2026-08-09 18:07:02

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Curadent Zellstofftupfer 4 x 5 cm?

The registered manufacturer of record for Curadent Zellstofftupfer 4 x 5 cm is Wilhelm Weisweiler GmbH & Co. KG.

What is the Primary UDI-DI identifier for Curadent Zellstofftupfer 4 x 5 cm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is EWWV182300031.

What classification code is assigned to this device?

This device is registered under product classification code M0199.

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