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Diamantstreifen

EUDAMED

Class I (EU MDR)

Ref FS3-SFXP

by NTI-Kahla GmbH Rotary Dental Instruments

Identity

Trade Name
Diamantstreifen EUDAMED
Device Name
Diamantstreifen EUDAMED
Model / Reference
FS3-SFXP EUDAMED

Identifiers

Primary DI / UDI-DI
+E310FS3SFXP1 EUDAMED
Basic UDI-DI
++E310DiaStFuellDF EUDAMED
Unit of Use DI
+E310FS3SFXP0 EUDAMED
EMDN Code
L159019 DENTAL FINISHING RASPS AND FILES, REUSABLE 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

Diamantstreifen by NTI - Kahla GmbH Rotary Dental Instruments — Class I — 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
DE-MF-000009451

Sources (1)

  • EUDAMED 733d2a79-545c-4935-9d9d-1244cc26becb 61 fields · synced Oct 9, 2026