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Tocular

EUDAMED

Class I (EU MDR)

Ref 4000056

by Haag-Streit AG

Identity

Trade Name
TOCULAR EUDAMED
Device Name
NEO 900 TOCULAR EUDAMED
Model / Reference
4000056 EUDAMED

Identifiers

Primary DI / UDI-DI
07640132987973 EUDAMED
Basic UDI-DI
764013298NEO900_TocularKD EUDAMED
Direct Marketing DI
07640132987973 EUDAMED
EMDN Code
Z1201118099 INSTRUMENTS FOR OPERATIVE MICROSCOPY - HARDWARE ACCESSORIES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Bulgaria 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

Tocular 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

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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 d91e28d8-5926-4fb5-ae61-5ddeba1c4f85 61 fields · synced Aug 1, 2026