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KeriKnife™ - Mini Surgical Knife

EUDAMED

Class IIa (EU MDR)

Ref 524-A80000

by Keri Medical SA

Identity

Trade Name
KeriKnife™ - Mini Surgical Knife EUDAMED
Device Name
KeriKnife EUDAMED
Model / Reference
524-A80000 EUDAMED

Identifiers

Primary DI / UDI-DI
07640181162321 EUDAMED
Basic UDI-DI
764018116005B4 EUDAMED
EMDN Code
V0199 CUTTING DEVICES, SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France 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

KeriKnife™ - Mini Surgical Knife by Keri Medical SA — 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
Keri Medical SA
EUDAMED SRN
CH-MF-000021960
Authorised Representative
Keri Medical France FR-AR-000009590

Sources (1)

  • EUDAMED 18b4157b-4708-42b8-a096-8f5f9e2a8232 61 fields · synced Jun 19, 2026