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A-Scan Probe 4SIGHT

EUDAMED

Class IIa (EU MDR)

Ref 24-8000ARef 24-4001

by Accutome Inc. DBA Keeler USA

Identity

Trade Name
A-Scan Probe 4SIGHT EUDAMED
A-Scan Probe EUDAMED
Device Name
A-Scan Probe 4Sight EUDAMED
A-Scan Probe EUDAMED
Model / Reference
24-8000A EUDAMED
24-4001 EUDAMED

Identifiers

Primary DI / UDI-DI
00897826002307 EUDAMED
00897826002321 EUDAMED
Basic UDI-DI
B-00897826002307 EUDAMED
B-00897826002321 EUDAMED
EMDN Code
Q0299 OPHTHALMIC DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria EUDAMED
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

A-Scan Probe 4SIGHT by Accutome Inc. DBA Keeler USA — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Manufacturer's product page: 4Sight system

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
US-MF-000036181
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 18869b9a-02ce-4644-b02f-4836a9e06bfb 61 fields · synced Jul 9, 2026
  • EUDAMED 60e6259e-532a-43a5-a4e0-e82f38d7df3d 61 fields · synced May 17, 2026