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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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CCR / CLR instrument IIa — 168 UDI-DI variants, MDR (Aesculap AG)

MD Atlas
Aesculap AG

Data from EUDAMED, last updated May 23, 2026

CCR / CLR instrument IIa

40392390000026122J

168 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: 40392390000026122J
Device name: CCR / CLR instrument IIa
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

168 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KC3NJ4M5NK7567E0G9DACS72

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

CLR04038653254651
CLR04038653254774
CLR04038653254644
CLR04038653220267
CLR04038653254729
CLR04038653254682
CLR04038653254736
CLR04038653254712
CLR04038653254750
CLR04038653324965
CLR04038653254675
CLR04038653254781
CLR04038653254699
CLR04038653324958
CLR04038653324972
CLR04038653254705
CLR04038653254767
CLR04038653254743

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