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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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THA profiler adapter/handle — 14 UDI-DI variants, MDR (Aesculap AG)

MD Atlas
Aesculap AG

Data from EUDAMED, last updated May 23, 2026

THA profiler adapter/handle

403923900000195134

14 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: 403923900000195134
Device name: THA profiler adapter/handle
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 25, 2025

Manufacturer & authorised representative

Manufacturer

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

Variants by status

UDI-DI variants

14 UDI-DI variants

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Applied filters

basicUdiUlid01KAWZY93FM40MAKKE51E65ZRC

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

Aesculap04046963626440
Aesculap04046963626457
Aesculap04046963653750
Aesculap04046963626433
Aesculap04046963653743
Aesculap04046963626471
Aesculap04046963626464
Aesculap04046964471940
Aesculap04046963626426
Aesculap04046963653767
Aesculap04046963626419
TRJ04046963643324
TRJ04046963643348
TRJ04046963643331