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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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TRJ preparation instrument — 27 UDI-DI variants, MDR (Aesculap AG)

MD Atlas
Aesculap AG

Data from EUDAMED, last updated May 23, 2026

TRJ preparation instrument

4039239000000415ZV

27 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: 4039239000000415ZV
Device name: TRJ preparation instrument
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 8, 2025

Manufacturer & authorised representative

Manufacturer

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

Variants by status

UDI-DI variants

27 UDI-DI variants

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Applied filters

basicUdiUlid01K71CPQS1KEVF1CK16D2N34KQ

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

TRJ04046963891961
TRJ04046963893705
TRJ04046963893835
TRJ04046963643416
TRJ04046963893866
TRJ04046963893859
TRJ04046963893750
TRJ04046963893828
TRJ04046963893774
TRJ04046963643447
TRJ04046963643362
TRJ04046963643379
TRJ04046963893743
TRJ04046963643409
TRJ04046963643461
TRJ04046963643423
TRJ04046963893736
TRJ04046963643393
TRJ04046963527044
TRJ04046963643386
TRJ04046963893811
TRJ04046963893767
TRJ04046963643478
TRJ04046963893781
TRJ04046963643454

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