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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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Acetabular reamer/Bipolar Cup trial head — 86 UDI-DI variants, MDR

MD Atlas
Aesculap AG

Data from EUDAMED, last updated May 23, 2026

Acetabular reamer/Bipolar Cup trial head

40392390000028543C

86 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: 40392390000028543C
Device name: Acetabular reamer/Bipolar Cup trial head
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

86 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KC3S2PTRFDZB6FJ140CJKEC2

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

Aesculap04038653114306
Aesculap04038653114351
Aesculap04038653115549
Aesculap04038653114337
Aesculap04038653114276
Aesculap04038653114313
Aesculap04038653447343
Aesculap04046963611675
Aesculap04046955280117
Aesculap04038653447268
Aesculap04038653114245

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