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Leica 819

EUDAMED

Class A (EU MDR)

Ref 14035838925

by Leica Biosystems Nussloch GmbH

Identity

Trade Name
Leica 819 EUDAMED
Device Name
Leica DB80 HS, LS, LX; 818, 819 EUDAMED
Model / Reference
14035838925 EUDAMED

Identifiers

Primary DI / UDI-DI
04049188114594 EUDAMED
Basic UDI-DI
010404918803589W EUDAMED
EMDN Code
V010302 BLADES WITHOUT SAFETY SYSTEMS, SINGLE-USE - NOT INCLUDED IN OTHER CLASSES EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Category: Manual scalpel blade, single-use

Leica 819 by Leica Biosystems Nussloch Gmbh — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Manual scalpel blade, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
DE-MF-000021943

Sources (1)

  • EUDAMED 911be767-b484-4a87-a54d-ba205e83fbde 61 fields · synced Jun 17, 2026