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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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Rhyk NEO — 4 UDI-DI variants, MDR (Rhyk Technologies GmbH)

MD Atlas
Rhyk Technologies GmbH

Data from EUDAMED, last updated May 23, 2026

Rhyk NEO

426074585RhykNEOR6

4 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: Rhyk Technologies GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426074585RhykNEOR6
Device name: Rhyk NEO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Aug 11, 2023

Manufacturer & authorised representative

Manufacturer

Name: Rhyk Technologies GmbH
SRN: DE-MF-000009068
Country: Germany
Email: v.tabrizi@rhyk.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H7HRKM3T8XF1Y358333ZAG5C

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

RH010204260745850216
RH010104260745850117
RH010004260745851619
RH010304260745850315