Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

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

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

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

11023804064295005443
110567-U104064295057039
11036804064295007171
110251-I04064295005627
110518-U304064295057497
11066004064295010287
11057904064295009458
11028504064295006044
11026704064295005863
11021404064295005061
110474-104064295057770
110205-U04064295004958
11052604064295008901
11058704064295009540
11023404064295005399
11057004064295009359
110922-A04064295012342
11045104064295008123
110914-A04064295012243
110101-A04064295003777
11023604064295005405
110118-U04064295003913
11026104064295005801
11033004064295006693
110530-204064295008949

4 5 6 7 8