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Stérilux® ES

EUDAMED

Class I (EU MDR)

Ref 241327Model 1082

by Laboratoires PAUL HARTMANN S.à.r.l

Identity

Trade Name
Stérilux® ES EUDAMED
Device Name
Stérilux ES EUDAMED
Model / Reference
1082 EUDAMED
241327 EUDAMED

Identifiers

Primary DI / UDI-DI
03261480000196 EUDAMED
Basic UDI-DI
32614810824C EUDAMED
EMDN Code
M020199 COTTON GAUZES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

Yes

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

Stérilux® ES by Laboratoires PAUL HARTMANN S.à.r.l — 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
FR-MF-000004029

Sources (1)

  • EUDAMED 16d66d68-0bd5-493e-9530-5d1ad8a6a91e 61 fields · synced Jun 20, 2026