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

MD Atlas
Aesculap AG

Data from EUDAMED, last updated May 23, 2026

Endoscope

40392390000027393B

20 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Aesculap AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 40392390000027393B
Device name: Endoscope
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Dec 10, 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

basicUdiUlid01KC3NHPNPACTM5QGYTK23DGFK

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

Aesculap04038653255672
Aesculap04038653300662
Aesculap04038653081370
Aesculap04038653255702
Aesculap04038653081400
Aesculap04038653314249
Aesculap04038653081394
Aesculap04038653081523
Aesculap04038653392810
Aesculap04038653081486
Aesculap04038653255689
Aesculap04038653081356
Aesculap04038653255696
Aesculap04038653081271
Aesculap04038653392827
Aesculap04038653081318
Aesculap04038653300679
Aesculap04038653081509
MINOP® TREND04046963313845
MINOP® TREND04046963313869