GUDIDData
eudamed_udi Primary ID: 04251610630637

Injektionskanüle 0,70 x 200 mm, Luer Lock (UDI 04251610630637)

Manufactured by Robert Helwig GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Injektionskanüle 0,70 x 200 mm, Luer Lock - Primary ID 04251610630637

Device Regulatory Overview

The Injektionskanüle 0,70 x 200 mm, Luer Lock (Model/Catalog Number: 32070200) is a medical device manufactured by Robert Helwig GmbH. This product is indexed under FDA Product Code / Category Classification A01010199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
32070200
Product Code / EMDN
A01010199
Device Name
Injektionskanülen unsteril zum Einmalgebrauch
Database Sync Date
2026-08-09 16:46:29

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 Injektionskanüle 0,70 x 200 mm, Luer Lock?

The registered manufacturer of record for Injektionskanüle 0,70 x 200 mm, Luer Lock is Robert Helwig GmbH.

What is the Primary UDI-DI identifier for Injektionskanüle 0,70 x 200 mm, Luer Lock?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251610630637.

What classification code is assigned to this device?

This device is registered under product classification code A01010199.

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