PediStick

by Pedistick Limited

Ref PediStick 101Model 101

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number50700031143PS1018R Basic UDI-DI 15070003114303UDI-DI	Date20 Jan 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Withdrawn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: PediStick
Model / Reference: 101, PediStick 101

Primary DI / UDI-DI: 15070003114303
Basic UDI-DI: 50700031143PS1018R
EMDN Code: L99 Surgical instruments, reusable - other

Device Class: Class I
EU market of registration: Netherlands

Manufacturer details

EUDAMED SRN: UK-MF-000045247
Authorised representative: Kingsmead Service B.V. NL-AR-000002066

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