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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

500 ml — Class I MDR by Laboratorios Kin SA

MD Atlas
Laboratorios Kin SA

EUDAMED last updated this device on Apr 22, 2026

500 ml

843602621KOS1DG

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Laboratorios Kin SA
UDI-DI code: 08436026215517
Reference / catalog number: 500 ml

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Manufacturer information

Organization name: Laboratorios Kin SA
SRN: ES-MF-000052658
Manufacturer status: Active

Critical warnings

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

CW011
This product is for external use only. Do not swallow. Keep out of the reach of children.

Market distribution

Primary placement in Spain; available across 2 countries total.

Country	On market since	Until
SpainPrimary placement	Oct 3, 2005	May 15, 2049
Portugal	Oct 3, 2005	May 15, 2049

Device identification

Trade name: not provided
UDI-DI code: 08436026215517
Basic UDI-DI: 843602621KOS1DG
Reference / catalog number: 500 ml
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

D0899DETERGENTS FOR MEDICAL 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

This device is not currently linked to any other device.

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.