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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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PS-Tools rotating instrument sterile SU — 61 UDI-DI variants, MDR

MD Atlas
Aesculap AG

Data from EUDAMED, last updated May 23, 2026

PS-Tools rotating instrument sterile SU

40392390000026753A

61 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: 40392390000026753A
Device name: PS-Tools rotating instrument sterile SU
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

61 UDI-DI variants

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Applied filters

basicUdiUlid01KC3QTSQJNG12Y33XP5ETZZ5J

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

HI-LINE XS04046963129187
HI-LINE XS04038653399079
HI-LINE XS04038653398768
HI-LINE XS04038653399086
HI-LINE XS04046963417482
HI-LINE XS04038653398546
HI-LINE XS04038653398744
HI-LINE XS04038653398447
HI-LINE XS04038653399116
HI-LINE XS04038653399093
HI-LINE XS04038653399154

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