eudamed_udi Primary ID: GNMBLK163PRO0

K3Pro Caps (UDI GNMBLK163PRO0)

Manufactured by Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The K3Pro Caps (Model/Catalog Number: MB.LK_1.6/3PRO) is a medical device manufactured by Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG. This product is indexed under FDA Product Code / Category Classification P01020101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: MB.LK_1.6/3PRO
Product Code / EMDN: P01020101
Device Name: K3Pro Caps
Database Sync Date: 2026-08-09 16:28:45

Full Regulatory Attributes

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{
    "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 K3Pro Caps?

The registered manufacturer of record for K3Pro Caps is Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG.

What is the Primary UDI-DI identifier for K3Pro Caps?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is GNMBLK163PRO0.

What classification code is assigned to this device?

This device is registered under product classification code P01020101.

Similar Classification Devices (P01020101)

Other Devices by Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG

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