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Monobloc reamer

EUDAMED

Class I (EU MDR)

Ref 311-A00500

by Keri Medical SA

Identity

Trade Name
Monobloc reamer EUDAMED
Device Name
Reamers EUDAMED
Model / Reference
311-A00500 EUDAMED

Identifiers

Primary DI / UDI-DI
07640181161775 EUDAMED
Basic UDI-DI
764018116016B9 EUDAMED
Direct Marketing DI
07640181161775 EUDAMED
EMDN Code
L091102 ORTHOPAEDIC PROSTHESES REAMERS AND BURS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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: Acetabular orthopaedic reamer

Monobloc reamer by Keri Medical SA — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Acetabular orthopaedic reamer.

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 0dda7da4-31c7-446b-936f-7aa700cf0aef 61 fields · synced Jul 21, 2026