Conical reamer ⌀ 9 mm

by Keri Medical SA

Ref 112-A21100

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number764018116016B9 Basic UDI-DI 07640181161164UDI-DI	Date29 Apr 2026Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name: Reamers
Model / Reference: 112-A21100

Primary DI / UDI-DI: 07640181161164
Basic UDI-DI: 764018116016B9
EMDN Code: L091102 Orthopaedic prostheses reamers and burs, reusable

Device Class: Class I
EU market of registration: France

Manufacturer details

EUDAMED SRN: CH-MF-000021960
Authorised representative: Keri Medical France FR-AR-000009590

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Properties

Reusable

Other properties (12)

Sterile: No
Implantable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No