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Kp-2007-25

EUDAMED

Class IIa (EU MDR)

Ref /Model KP,DM: 1006, 1008, 12vt, 1302, 1403, 1506, 1602, 1603, 1606, 16vt, 1704, 1705, 1708, 1712, 1805, 1902, 2004, 2005, 2006, 2007, 2205, 2206, 2504, 2506, 2508, 3002, 3004, 3006, 3009, 3502, 3504, 3506, 4002, 4004, 4006, 4502, 4503, 4504, 5002, 5004, 6002, E

by Guilin Kevin Peter Technology Co., Ltd.

Identity

Trade Name
KP-2007-25 EUDAMED
Device Name
Root Canal File EUDAMED
Model / Reference
KP,DM: 1006, 1008, 12vt, 1302, 1403, 1506, 1602, 1603, 1606, 16vt, 1704, 1705, 1708, 1712, 1805, 1902, 2004, 2005, 2006, 2007, 2205, 2206, 2504, 2506, 2508, 3002, 3004, 3006, 3009, 3502, 3504, 3506, 4002, 4004, 4006, 4502, 4503, 4504, 5002, 5004, 6002, E EUDAMED
/ EUDAMED

Identifiers

Primary DI / UDI-DI
06975384337414 EUDAMED
Basic UDI-DI
69753843302YN EUDAMED
EMDN Code
L159004 ENDODONTIC RASPS AND FILES, REUSABLE EUDAMED

Classification

Device Class
Class IIa 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

Kp-2007-25 by Guilin Kevin Peter Technology Co., Ltd. — 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

Manufacturer
Guilin Kevin Peter Technology Co., Ltd.
EUDAMED SRN
CN-MF-000022934
Authorised Representative
MedNet EC-REP C IIb GmbH DE-AR-000011194

Sources (1)

  • EUDAMED 1a03c9f2-8359-4c6e-aa05-d2c549375d4d 61 fields · synced Jun 19, 2026