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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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Wire grasping forceps — 20 UDI-DI variants, MDR (Aesculap AG)

MD Atlas
Aesculap AG

Data from EUDAMED, last updated May 23, 2026

Wire grasping forceps

403923900000033725

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

Reusable

Identity & classification

Basic UDI-DI: 403923900000033725
Device name: Wire grasping forceps
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 16, 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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Export results

Applied filters

basicUdiUlid01K58P5D3A7H2HT3RM3HF6ZZKT

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

Aesculap04038653050116
Aesculap04038653050079
Aesculap04038653050093
Aesculap04038653411184
Aesculap04038653174980
Aesculap04038653050086
Aesculap04038653050109
Aesculap04038653174966
Aesculap04038653174898
DUROGRIP®04038653028481
DUROGRIP®04038653392803
DUROGRIP®04038653028474
DUROGRIP®04038653028467
DUROGRIP®04038653139682
DUROGRIP®04038653174911
DUROGRIP®04038653174904
SQ.line®04046955285877
SQ.line®04046955285679
SQ.line®04046955282739
SQ.line®04046955285839