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Rigid Probe

EUDAMED

Class IIa (EU MDR)

Ref 202-3023

by Xiros Limited

Identity

Trade Name
Rigid Probe EUDAMED
Device Name
Rigid Probe EUDAMED
Probes EUDAMED
Model / Reference
202-3023 EUDAMED

Identifiers

Primary DI / UDI-DI
05060267132673 EUDAMED
05060267132918 EUDAMED
05060267133250 EUDAMED
Basic UDI-DI
B-05060267132673 EUDAMED
B-05060267132918 EUDAMED
506026713Probes00000000VW EUDAMED
EMDN Code
P091399 ORTHOPAEDIC IMPLANT INSTRUMENTS, SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Norway EUDAMED
Poland EUDAMED
Spain 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: Joint prosthesis implantation kit, single-use

Rigid Probe by Xiros Limited — Class IIa — MDR, MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Joint prosthesis implantation kit, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Xiros Limited
EUDAMED SRN
GB-MF-000004396
Authorised Representative
Advena Limited MT-AR-000000234

Sources (3)

  • EUDAMED f3435ea3-fe58-4474-9e5f-b88d22b372ea 61 fields · synced Jul 13, 2026
  • EUDAMED 73a56763-562f-4d53-a088-112fce3f4835 61 fields · synced May 19, 2026
  • EUDAMED 5d5d7a5b-4d9e-40ba-990e-18a3f32ce4e0 61 fields · synced May 19, 2026