← Back to catalogue

Elara 900 VS

EUDAMED

Class I (EU MDR)

Ref 1421007Model Elara

by Haag-Streit AG

Identity

Device Name
Elara 900 VS EUDAMED
Model / Reference
Elara EUDAMED
1421007 EUDAMED

Identifiers

Primary DI / UDI-DI
07640132988925 EUDAMED
Basic UDI-DI
764013298ElaraQD EUDAMED
Direct Marketing DI
07640132988925 EUDAMED
EMDN Code
Z12120108 SLIT LAMPS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

Elara 900 VS by Haag-Streit AG — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED 97d976ee-3f60-47a8-930d-5679ca3acfbf 61 fields · synced Jul 21, 2026