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NeoBurr

EUDAMED

Class IIa (EU MDR)

Ref FG.TC 245SS

by Microcopy, A Division of Neo-Flo, Inc.

Identity

Trade Name
NeoBurr EUDAMED
Device Name
Tungsten carbide Burs – Pre-Sterile EUDAMED
Model / Reference
FG.TC 245SS EUDAMED

Identifiers

Primary DI / UDI-DI
00840221631726 EUDAMED
Basic UDI-DI
08402216NBSMUDP EUDAMED
EMDN Code
Z12110102 DENTAL DRILLS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

Yes

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

NeoBurr by Microcopy, A Division of Neo-Flo, Inc. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
US-MF-000012637
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 23ffcf50-fd2e-499f-89ac-8370e775024f 61 fields · synced Sep 18, 2026