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Neolook S2S Professional

EUDAMED

Class I (EU MDR)

Ref PRO-DIG-100Model S2S Professional 2.0

by Neolook Solutions

Identity

Trade Name
Neolook S2S Professional EUDAMED
Device Name
Neolook S2S Professional EUDAMED
Model / Reference
S2S Professional 2.0 EUDAMED
PRO-DIG-100 EUDAMED

Identifiers

Primary DI / UDI-DI
08720299947726 EUDAMED
Basic UDI-DI
87202999477S2SProfK7 EUDAMED
Direct Marketing DI
08720299947726 EUDAMED
EMDN Code
V0299 NEONATOLOGY AND PAEDIATRIC DEVICES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Special Device Type
Software EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Assistive crawler/mobility board

Neolook S2S Professional by Neolook Solutions — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Assistive crawler/mobility board.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Neolook Solutions
EUDAMED SRN
NL-MF-000028851

Sources (1)

  • EUDAMED a9fd203e-432c-4e8c-9166-c743df4a516d 61 fields · synced Jun 18, 2026