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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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Organization name
UDI-DI code
Reference / catalog number

RH0103 — Class IIa MDR by Rhyk Technologies GmbH

MD Atlas
Rhyk Technologies GmbH

EUDAMED last updated this device on Aug 11, 2023

RH0103

426074585RhykNEOR6

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Rhyk Technologies GmbH
UDI-DI code: 04260745850315
Reference / catalog number: RH0103

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Manufacturer information

Organization name: Rhyk Technologies GmbH
SRN: DE-MF-000009068
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
For contra-indications. see instructions for use

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Sep 1, 2023	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260745850315
Basic UDI-DI: 426074585RhykNEOR6
Reference / catalog number: RH0103
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Rhyk NEO is used for the treatment and relief of pain, as well as for the treatment and compensation of muscular restrictions, injuries and disabilities caused by diseases, through the application of electromyostimulation and electrotherapy (muscular and nervous) to the human body. This set is delivered with Rhyk NEOBACK size XL.
Additional information URL: https://www.rhyk.com/downloads/HF-RHYK-NEO-REC-16-DE_IFU_V10.pdf
Clinical sizes: XL

EMDN nomenclature code(s)

N99NERVOUS AND MEDULLARY SYSTEM DEVICES - OTHER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

RH0102426074585RhykNEOR6On the market RH0101426074585RhykNEOR6On the market RH0100426074585RhykNEOR6On the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.