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Octopus 600

EUDAMED

Class IIa (EU MDR)

Ref 1806000

by Haag-Streit AG

Identity

Trade Name
Octopus 600 EUDAMED
Device Name
Octopus 600 EUDAMED
Model / Reference
1806000 EUDAMED

Identifiers

Primary DI / UDI-DI
07640132985443 EUDAMED
Basic UDI-DI
B-07640132985443 EUDAMED
EMDN Code
Z1212012001 VISUAL FUNCTIONAL ASSESSMENT EQUIPMENT EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Octopus 600 by Haag-Streit AG — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Haag-Streit AG
EUDAMED SRN
CH-MF-000020981
Authorised Representative
Haag-Streit Deutschland GmbH DE-AR-000025462

Sources (1)

  • EUDAMED 6e693318-ab2b-4f04-a73a-c4a5761efea4 61 fields · synced Jul 19, 2026