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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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TGN-R100GR — 8 UDI-DI variants, MDR (Rolko Kohlgrüber GmbH)

MD Atlas
Rolko Kohlgrüber GmbH

Data from EUDAMED, last updated May 23, 2026

TGN-R100GR

426067605TGN-R100GR0000CU

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: 426067605TGN-R100GR0000CU
Device name: TGN-R100GR
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

basicUdiUlid01FMA70ZX709VQMWT3RE4Z7BSV

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

TGN-R100GR-0104260676053564
TGN-R100GR04260676050013
TGN-R100GR-HR-104260676050068
TGN-R100GR-L204260676050105
TGN-R100GR-HR-1-55/6004260676050082
TGN-R100GR-BO04260676050020
TGN-R100GR-WB-0104260676050129
TGN-R100GR-CO04260676050044