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56210A Kreissig Localizer

EUDAMED

Class I (EU MDR)

Ref 56210A

by Bausch & Lomb GmbH

Identity

Trade Name
56210A Kreissig Localizer EUDAMED
Device Name
Reusable devices EUDAMED
Model / Reference
56210A EUDAMED

Identifiers

Primary DI / UDI-DI
04058935007997 EUDAMED
Basic UDI-DI
4058935-000000-AC EUDAMED
Direct Marketing DI
04058935007997 EUDAMED
EMDN Code
L170102 OCULAR AND ENDOCULAR RETRACTORS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands 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

56210A Kreissig Localizer by Bausch & Lomb GmbH — 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
Bausch & Lomb GmbH
EUDAMED SRN
DE-MF-000009142

Sources (1)

  • EUDAMED 974f3f69-cf42-409c-b761-89cb2eddf003 61 fields · synced Jun 19, 2026