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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

100 ml — Class I MDR by Laboratorios Kin SA

MD Atlas
Laboratorios Kin SA

EUDAMED last updated this device on May 28, 2026

100 ml

843602621KOS1DG

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Laboratorios Kin SA
UDI-DI code: 08436026215524
Reference / catalog number: 100 ml

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View device family (Basic UDI)

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.

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Market distribution

Primary placement in Spain; available across 2 countries total.

Country	On market since	Until
SpainPrimary placement	Feb 1, 2006	May 15, 2049
Portugal	Feb 1, 2006	May 15, 2049

Device identification

Trade name: not provided
UDI-DI code: 08436026215524
Basic UDI-DI: 843602621KOS1DG
Reference / catalog number: 100 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.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

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

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Related devices

500 ml843602621KOS1DGOn 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.