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SK PODO 10 mm rund / round orange grob / coarse

EUDAMED

Class I (EU MDR)

Ref A21100102080Ref A21100102080A

by LUKAS-ERZETT GmbH & Co.KG

Identity

Trade Name
SK PODO 10 mm rund / round orange grob / coarse EUDAMED
Device Name
SK PODO, SK THERMO, GT PODO, GT SPECIAL EUDAMED
Model / Reference
A21100102080 EUDAMED
A21100102080A EUDAMED

Identifiers

Primary DI / UDI-DI
04027497600069 EUDAMED
04027497260584 EUDAMED
Basic UDI-DI
4027497113115WB EUDAMED
Unit of Use DI
14027497600066 EUDAMED
14027497608055 EUDAMED
EMDN Code
V0199 CUTTING DEVICES, SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

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

Category: Cranial bur, single-use

SK PODO 10 mm rund / round orange grob / coarse by LUKAS-ERZETT GmbH & Co.KG — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Cranial bur, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
DE-MF-000005344

Sources (2)

  • EUDAMED 18198ed6-c88a-437c-946e-80a1bcbeffc4 61 fields · synced Jul 29, 2026
  • EUDAMED c31b7b4b-feb6-4bfe-bb32-1d2cf1934022 61 fields · synced May 19, 2026