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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

Copi Stroke V1.0 — Class I MDR by Copimed GmbH

MD Atlas
Copimed GmbH

EUDAMED last updated this device on Feb 3, 2026

Copi Stroke V1.0

PP1446531516961

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Copimed GmbH
UDI-DI code: 1314465315169050
Reference / catalog number: Copi Stroke V1.0

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Manufacturer information

Organization name: Copimed GmbH
SRN: DE-MF-000050277
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 1314465315169050
Basic UDI-DI: PP1446531516961
Reference / catalog number: Copi Stroke V1.0
Issuing entity: IFA

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: Die Software Copi Stroke dient der strukturierten Erfassung, Dokumentation und Organisation klinischer Abläufe in Stroke Units.
Additional information URL: https://copimed.de/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V92MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES

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.