← Back to catalogue

SK THERMO 7 mm spitz / pointed grob / coarse

EUDAMED

Class I (EU MDR)

Ref A21080073080

by LUKAS-ERZETT GmbH & Co.KG

Identity

Trade Name
SK THERMO 7 mm spitz / pointed grob / coarse EUDAMED
Device Name
SK PODO, SK THERMO, GT PODO, GT SPECIAL EUDAMED
Model / Reference
A21080073080 EUDAMED

Identifiers

Primary DI / UDI-DI
04027497609451 EUDAMED
Basic UDI-DI
4027497113115WB EUDAMED
Unit of Use DI
14027497609458 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 THERMO 7 mm spitz / pointed 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
DE-MF-000005344

Sources (1)

  • EUDAMED 8fe6afd3-2b20-4f9d-ac77-4b17a05b84af 61 fields · synced Jul 22, 2026