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H-6038

EUDAMED

Class I (EU MDR)

Ref H-6038Model Forceps

by Albert Heiss GmbH & Co. KG

Identity

Model / Reference
Forceps EUDAMED
H-6038 EUDAMED

Identifiers

Primary DI / UDI-DI
04250326815369 EUDAMED
Basic UDI-DI
4250326800010012WQ EUDAMED
Direct Marketing DI
04250326815369 EUDAMED
EMDN Code
L170201 OPHTHALMIC GRASPING FORCEPS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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-6038 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 8361a6c1-5541-4e5d-9cb2-479fd3cd6dfb 61 fields · synced Jul 8, 2026