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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

412681-004 — Class I MDR by AirLife Finland Oy

MD Atlas
AirLife Finland Oy

EUDAMED last updated this device on May 26, 2025

412681-004

088948320041cECGmon138

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: AirLife Finland Oy
UDI-DI code: 10889483582695
Reference / catalog number: 412681-004

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Manufacturer information

Organization name: AirLife Finland Oy
SRN: FI-MF-000001482
Manufacturer status: Active

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

2 warnings recorded — scroll inside the panel to see all entries.

CW027
Do not use this product in MRI environment.
CW011
Products are supplied non-sterile and must be unpacked, cleaned and disinfected prior to first use. Products must be reprocessed prior to each use.

Market distribution

Primary placement in Finland; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 10889483582695
Basic UDI-DI: 088948320041cECGmon138
Reference / catalog number: 412681-004
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)

Z12050380ELECTROCARDIOGRAPHS - HARDWARE ACCESSORIES

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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