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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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Bone cutting forceps — 21 UDI-DI variants, MDR (Aesculap AG)

MD Atlas
Aesculap AG

Data from EUDAMED, last updated May 23, 2026

Bone cutting forceps

403923900000169335

21 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

Reusable

Identity & classification

Basic UDI-DI: 403923900000169335
Device name: Bone cutting forceps
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
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

21 UDI-DI variants

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Applied filters

basicUdiUlid01KAB0V0TMNTDRCMBJPC4B9R5J

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

Aesculap04038653169108
Aesculap04038653169115
Aesculap04038653169146
Aesculap04038653047864
Aesculap04038653169092
Aesculap04038653047857
Aesculap04038653047925
Aesculap04038653047901
Aesculap04038653169122
Aesculap04038653047918
Aesculap04038653169078
Aesculap04038653169139
Aesculap04038653047833
Aesculap04038653169085
Aesculap04038653047871
Aesculap04038653047932
Aesculap04038653047840
Aesculap04038653047826
Aesculap04038653169061
SQ.line®04046955282586
SQ.line®04046955285808