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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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PROSPACE/TSPACE instrument tray — 14 UDI-DI variants, MDR

MD Atlas
Aesculap AG

Data from EUDAMED, last updated May 23, 2026

PROSPACE/TSPACE instrument tray

40392390000006192J

14 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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 40392390000006192J
Device name: PROSPACE/TSPACE instrument tray
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 19, 2026

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

basicUdiUlid01KFB1PTJ21GFEQSZDRT7A93YN

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

PROSPACE04046963954987
PROSPACE 3D04046955328710
PROSPACE 3D04046955327249
PROSPACE 3D04046955328727
PROSPACE 3D04046955327256
PROSPACE OBLIQUE 3D04046955328741
PROSPACE TITANIUM04046964104336
PROSPACE TITANIUM04046964104329
TSPACE04046963575922
TSPACE04046963575915
TSPACE04046963776053
TSPACE 3D04046955328765
TSPACE PEEK/XP04046964553912
TSPACE PEEK/XP04046964553929