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Lynxera Xa35

EUDAMED

Class A (EU MDR)

Ref 10074723

by Lutz GmbH & Co. KG

Identity

Trade Name
LYNXERA XA35 EUDAMED
Device Name
LYNXERA LS35, LN35, LA35, XA35, XN35, XS35 EUDAMED
Model / Reference
10074723 EUDAMED

Identifiers

Primary DI / UDI-DI
04260758240462 EUDAMED
Basic UDI-DI
4260758246067YZ 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

Lynxera Xa35 by Lutz GmbH & Co. KG — 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

Manufacturer
Lutz GmbH & Co. KG
EUDAMED SRN
DE-MF-000038332

Sources (1)

  • EUDAMED c7d1cc50-6e1c-4f67-98e2-8ae812606d2d 61 fields · synced Jul 10, 2026