GUDIDData
eudamed_udi Primary ID: 04251610630293

Injektionskanüle 0,60 x 80 mm, Luer Lock (UDI 04251610630293)

Manufactured by Robert Helwig GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Injektionskanüle 0,60 x 80 mm, Luer Lock - Primary ID 04251610630293

Device Regulatory Overview

The Injektionskanüle 0,60 x 80 mm, Luer Lock (Model/Catalog Number: 32060080) 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
32060080
Product Code / EMDN
A01010199
Device Name
Injektionskanülen unsteril zum Einmalgebrauch
Database Sync Date
2026-08-09 16:29:07

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 Injektionskanüle 0,60 x 80 mm, Luer Lock?

The registered manufacturer of record for Injektionskanüle 0,60 x 80 mm, Luer Lock is Robert Helwig GmbH.

What is the Primary UDI-DI identifier for Injektionskanüle 0,60 x 80 mm, Luer Lock?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251610630293.

What classification code is assigned to this device?

This device is registered under product classification code A01010199.

Programmatic Export

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

JSON API Endpoint