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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Tray — 3 UDI-DI variants, MDR (MEDIGMA BIOMEDICAL GMBH)

MD Atlas
MEDIGMA BIOMEDICAL GMBH

Data from EUDAMED, last updated May 23, 2026

Tray

426052516EmptyKitDC

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: MEDIGMA BIOMEDICAL GMBH

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 426052516EmptyKitDC
Device name: —
Device model: Tray
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 24, 2024

Manufacturer & authorised representative

Manufacturer

Name: MEDIGMA BIOMEDICAL GMBH
SRN: DE-MF-000009412
Country: Germany
Email: office@medigma-implants.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HMY1ST7NWJ9EJ9YMQSNQDX9H

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

Fix Konisch Surgical Tray04260525163581
Surgery Kit - Plastic Tray04260525167442
Surgery Kit Standard Hex - Plastic Tray04260525167435