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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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Aufrichtgriff ECOgrip — 8 UDI-DI variants, MDR (Rolko Kohlgrüber GmbH)

MD Atlas
Rolko Kohlgrüber GmbH

Data from EUDAMED, last updated May 23, 2026

Aufrichtgriff ECOgrip

426067605TGE00000000000J9

8 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: 426067605TGE00000000000J9
Device name: Aufrichtgriff ECOgrip
Device model: TGE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 12, 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

8 UDI-DI variants

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Applied filters

basicUdiUlid01FM506JZJVNGSC96N35BMJNEW

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

TGE-RSG100-104260676050303
TGE-RSG70-L04260676050341
TGE-RSG70-HMS04260676051348
TGE-SVG11004260676050365
TGE-RSG70-0104260676050327
TGE-SVG85-DMA04260676050389
TGE-RSG70-WM04260676051584
TGE-RG43004260676052451