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CellRemo

EUDAMED

Class IIa (EU MDR)

Ref CLR_01KR

by Kims Med Co., Ltd.

Identity

Trade Name
CellRemo EUDAMED
Model / Reference
CLR_01KR EUDAMED

Identifiers

Primary DI / UDI-DI
08800071700463 EUDAMED
Basic UDI-DI
88000717CLR_01KRUQ EUDAMED
EMDN Code
V0199 CUTTING DEVICES, SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

Yes

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

CellRemo by Kims Med Co., Ltd. — Class IIa — 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

Manufacturer
Kims Med Co., Ltd.
EUDAMED SRN
KR-MF-000022749
Authorised Representative
Specculo Limited MT-AR-000034988

Sources (1)

  • EUDAMED 1b975f20-54af-42a9-a57b-9dc16b29a940 61 fields · synced Jun 18, 2026