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H-1071

EUDAMED

Class I (EU MDR)

Ref H-1071Model Eye Speculum

by Albert Heiss GmbH & Co. KG

Identity

Model / Reference
Eye Speculum EUDAMED
H-1071 EUDAMED

Identifiers

Primary DI / UDI-DI
04250326800457 EUDAMED
Basic UDI-DI
4250326800010018X4 EUDAMED
Direct Marketing DI
04250326800457 EUDAMED
EMDN Code
L170102 OCULAR AND ENDOCULAR RETRACTORS, REUSABLE 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

H-1071 by Albert Heiss GmbH & Co. KG — 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

EUDAMED SRN
DE-MF-000005495

Sources (1)

  • EUDAMED bab80494-5a48-4f8a-b0ee-0f3d5e0d3db1 61 fields · synced Sep 17, 2026