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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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ABC implantation instrument IIa RU — 13 UDI-DI variants, MDR

MD Atlas
Aesculap AG

Data from EUDAMED, last updated May 23, 2026

ABC implantation instrument IIa RU

40392390000005442C

13 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: 40392390000005442C
Device name: ABC implantation instrument IIa RU
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 18, 2025

Manufacturer & authorised representative

Manufacturer

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

Variants by status

UDI-DI variants

13 UDI-DI variants

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Applied filters

basicUdiUlid01KAB2BBTZ3Z1010GEEZ72XK96

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

ABC04038653377572
ABC04038653200887
ABC04038653397006
ABC04038653200832
ABC04038653422883
ABC04038653200825
ABC04038653253074
ABC04038653422890
ABC04038653327201
ABC E-PLATE04038653304899
ABC204038653449941
ABC204038653449934
ABC204038653405596