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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

00270EBG000 — Class I MDR by Reiner Medtech S.L.U

MD Atlas
Reiner Medtech S.L.U

EUDAMED last updated this device on Sep 17, 2025

00270EBG000

8437028850URI1000000110FJ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Reiner Medtech S.L.U
UDI-DI code: 08437028850003
Reference / catalog number: 00270EBG000

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Manufacturer information

Organization name: Reiner Medtech S.L.U
SRN: ES-MF-000048477
Manufacturer status: Active

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Spain; available across 1 country total.

Placed on the market in Spain; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 08437028850003
Basic UDI-DI: 8437028850URI1000000110FJ
Reference / catalog number: 00270EBG000
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: URICLAK® es un dispositivo controlador externo transformable para la incontinencia urinaria masculina, práctico y fácil de usar. Tiene forma de anillo aplastado, que al presionarlo lateralmente con dos dedos se transforma en un anillo de forma circular, permitiendo orinar sin necesidad de sacarlo del pene ni de desmontarlo, evitando salpicaduras.
Additional information URL: https://www.uriclak.com/dispositivo-para-incontinencia-urinaria-masculina.html
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

T0499INCONTINENCE 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

00540EAM030 8437028850CIM1000000110HUOn the market 00540EAZ010 8437028850CIM1000000110HUOn the market 00540ENA030 8437028850CIM1000000110HUOn the market 00540EAM010 8437028850CIM1000000110HUOn the market 00540EAZ030 8437028850CIM1000000110HUOn 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.