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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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Kopfstützenhalter — 13 UDI-DI variants, MDR (Rolko Kohlgrüber GmbH)

MD Atlas
Rolko Kohlgrüber GmbH

Data from EUDAMED, last updated May 23, 2026

Kopfstützenhalter

426067605KSH00000000000QZ

13 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: Rolko Kohlgrüber GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426067605KSH00000000000QZ
Device name: Kopfstützenhalter
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 26, 2021

Manufacturer & authorised representative

Manufacturer

Name: Rolko Kohlgrüber GmbH
SRN: DE-MF-000005748
Country: Germany
Email: info@rolko.com

Variants by status

UDI-DI variants

13 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FNDYSCY9T3420EJ4496R6HY0

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

HA-KO-ALU-C2204260676051775
PU-KO-6-S04260676051874
HA-KO-ALU-KG-C2204260676051799
PU-KO-5-S04260676051867
PU-KO-7-S04260676051881
HA-KO-ALU-C2504260676051782
HA-KO-ALU-R04260676051836
HA-UV-KO-38-S04260676051829
HA-KO-ALU-KG-C2504260676051805
U-BV-KOU-S04260676051850
HA-UV-KO-S04260676051812
PU-KO-10-S04260676051911
HA-KO-ALU-KG04260676051843