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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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PLASMACUP Screw Cup instrument — 11 UDI-DI variants, MDR (Aesculap AG)

MD Atlas
Aesculap AG

Data from EUDAMED, last updated May 23, 2026

PLASMACUP Screw Cup instrument

40392390000025512P

11 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: 40392390000025512P
Device name: PLASMACUP Screw Cup instrument
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

11 UDI-DI variants

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Applied filters

basicUdiUlid01KC3QTQ6BZC039N4MAP6BYQ4N

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

Aesculap04038653205912
Aesculap04038653110155
Aesculap04038653205851
Aesculap04038653435517
Aesculap04038653205868
Aesculap04038653205905
Aesculap04038653205875
Aesculap04038653205899
Aesculap04038653205882
PLASMACUP04038653112524
PLASMACUP04038653112531