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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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AMED — 607 UDI-DI variants, MDR (Akkuplanet GmbH)

MD Atlas
Akkuplanet GmbH

Data from EUDAMED, last updated May 23, 2026

AMED

4064295AMEDX6

607 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: Akkuplanet GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4064295AMEDX6
Device name: AMED
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 15, 2025

Manufacturer & authorised representative

Manufacturer

Name: Akkuplanet GmbH
SRN: DE-MF-000011648
Country: Germany
Email: info@akkuplanet.de
Phone: +4921599224000

Variants by status

UDI-DI variants

607 UDI-DI variants

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Applied filters

basicUdiUlid01K2PXW3EGN0CVDK4WY8G38MCS

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

11005004064295003180
110425-I04064295007843
110031-104064295002985
110385-U04064295007379
11059704064295009649
11029304064295006112
110232-U04064295005375