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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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Storage basket — 20 UDI-DI variants, MDR (Aesculap AG)

MD Atlas
Aesculap AG

Data from EUDAMED, last updated May 23, 2026

Storage basket

403923900000115626

20 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: Aesculap AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 403923900000115626
Device name: Storage basket
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 21, 2025

Manufacturer & authorised representative

Manufacturer

Name: Aesculap AG
SRN: DE-MF-000005504
Country: Germany
Email: eudamed@bbraun.com

Variants by status

UDI-DI variants

20 UDI-DI variants

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Applied filters

basicUdiUlid01K83HWKJK5BCWFDPDV1AAX30K

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

Aesculap04046963142469
Aesculap04046963093228
Aesculap04046963794590
Aesculap04046963093204
Aesculap04046963093211
Aesculap04038653126859
Aesculap04038653126866
Aesculap04046963142421
Aesculap04046964227790
Aesculap04038653263370
KAIRISON04046963150976
KAIRISON04046963409029
MINOP®04038653126880
MINOP®04038653200337
MINOP® InVent04046964058851
MINOP® InVent04046964058868
MINOP® TREND04046963363369
PaediScope®04038653320417
Yasargil®04046964982941
Yasargil®04046964982880