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Neolook S2S Family

EUDAMED

Class I (EU MDR)

Ref S2SFamModel 2.0

by Neolook Solutions

Identity

Trade Name
Neolook S2S Family EUDAMED
Device Name
Neolook S2S Family EUDAMED
Model / Reference
2.0 EUDAMED
S2SFam EUDAMED

Identifiers

Primary DI / UDI-DI
08720299947702 EUDAMED
Basic UDI-DI
87202999477S2SAA EUDAMED
Direct Marketing DI
08720299947702 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 Family 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 827cb442-c017-48a9-b7a0-2023e5d531e0 61 fields · synced Jul 28, 2026