GUDIDData
eudamed_udi Primary ID: 04260402645414

BePa-Clip VARIO 36/K, Musterpackung (UDI 04260402645414)

Manufactured by Novo Klinik-Service GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BePa-Clip VARIO 36/K, Musterpackung - Primary ID 04260402645414

Device Regulatory Overview

The BePa-Clip VARIO 36/K, Musterpackung (Model/Catalog Number: 801 702) is a medical device manufactured by Novo Klinik-Service GmbH. This product is indexed under FDA Product Code / Category Classification R01058099 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
801 702
Product Code / EMDN
R01058099
Device Name
Kanülenhalteband
Database Sync Date
2026-08-09 16:29:05

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 BePa-Clip VARIO 36/K, Musterpackung?

The registered manufacturer of record for BePa-Clip VARIO 36/K, Musterpackung is Novo Klinik-Service GmbH.

What is the Primary UDI-DI identifier for BePa-Clip VARIO 36/K, Musterpackung?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260402645414.

What classification code is assigned to this device?

This device is registered under product classification code R01058099.

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