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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

Efferon® NEO — Class IIb MDR by Efferon OÜ

MD Atlas
Efferon OÜ

EUDAMED last updated this device on Apr 16, 2026

Efferon® NEO

47450110216EfferonLPS7K

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Efferon OÜ
UDI-DI code: 04745011021656
Reference / catalog number: REF 24LEU002

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Manufacturer information

Organization name: Efferon OÜ
SRN: EE-MF-000024299
Manufacturer status: Active

Critical warnings

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

CW010
-
CW009
-
CW001
-
CW007
-
CW011
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Estonia; available across 2 countries total.

Country	On market since	Until
EstoniaPrimary placement		Still on market
Germany	Apr 7, 2026	Still on market

Device identification

Trade name: Efferon® NEO
UDI-DI code: 04745011021656
Basic UDI-DI: 47450110216EfferonLPS7K
Reference / catalog number: REF 24LEU002
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Device is intended for extracorporeal purification of blood by selective adsorption of lipopolysaccharides and non-selective adsorption of cytokines, myoglobin, cellular debris, endogenous and exogenous toxic substances. Efferon® is a non-pyrogenic, gamma-sterilized, single-use device.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

C03010104EXTRACORPOREAL CIRCULATION FILTERS

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

Efferon® LPS47450110216EfferonLPS7KOn 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.