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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

521018 — Class I MDR by Kimetec GmbH

MD Atlas
Kimetec GmbH

EUDAMED last updated this device on May 18, 2026

521018

42503736001KC

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Kimetec GmbH
UDI-DI code: 14250373655915
Reference / catalog number: 521018

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Manufacturer information

Organization name: Kimetec GmbH
SRN: DE-MF-000006493
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 14250373655915
Basic UDI-DI: 42503736001KC
Reference / catalog number: 521018
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: 4
Additional product description: Medical device for temporary use to apply pressure to peripheral blood vessels.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 35 MU50

EMDN nomenclature code(s)

V9003TOURNIQUETS

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

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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.