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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

ECM 5.1.18 — Class I MDD by Innoforce Anstalt

MD Atlas
Innoforce Anstalt

EUDAMED last updated this device on Sep 12, 2025

ECM 5.1.18

B-ECM-5.1.186N

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Innoforce Anstalt
UDI-DI code: D-ECM-5.1.186N
Reference / catalog number: ECM 5.1.18

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View device family (Basic UDI)

Manufacturer information

Organization name: Innoforce Anstalt
SRN: LI-MF-000002047
Manufacturer status: Active

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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.

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Austria; available across 2 countries total.

Country	On market since	Until
AustriaPrimary placement	Sep 27, 2024	Still on market
Germany	Sep 27, 2024	Still on market

Device identification

Trade name: not provided
UDI-DI code: D-ECM-5.1.186N
Basic UDI-DI: B-ECM-5.1.186N
Reference / catalog number: ECM 5.1.18
Issuing entity: EUDAMED

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Eye Clinic Manager (ECM) Version 5.1.18 Dragonfruit
Additional information URL: https://www.innoforce.com/en/products/
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

D-ECM-5.1.186N

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

EMDN nomenclature code(s)

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

Z12129092VARIOUS OPHTALMOLOGY INSTRUMENTS - MEDICAL DEVICE SOFTWARE
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

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