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GT PODO 5 mm konisch/conical Schaft 2, 35 X 40

EUDAMED

Class I (EU MDR)

Ref A25100512Ref A651005120026

by LUKAS-ERZETT GmbH & Co.KG

Identity

Trade Name
GT PODO 5 mm konisch/conical Schaft 2,35 X 40 EUDAMED
GT PODO 5 mm konisch/conical Schaft 2,35 X 35 EUDAMED
Device Name
SK PODO, SK THERMO, GT PODO, GT SPECIAL EUDAMED
Model / Reference
A25100512 EUDAMED
A651005120026 EUDAMED

Identifiers

Primary DI / UDI-DI
04027497074341 EUDAMED
04027497078394 EUDAMED
Basic UDI-DI
4027497113115WB 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

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

Category: Cranial bur, single-use

GT PODO 5 mm konisch/conical Schaft 2, 35 X 40 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 67b4dba7-ebf2-45d2-9246-ffa9242a0a0e 61 fields · synced Jul 18, 2026
  • EUDAMED a619bab2-d2fe-4473-9260-8624350b4ef1 61 fields · synced May 17, 2026