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Blunt pin

EUDAMED

Class IIa (EU MDR)

Ref 400425-002

by SI-BONE, Inc.

Identity

Device Name
Blunt pin EUDAMED
Model / Reference
400425-002 EUDAMED

Identifiers

Primary DI / UDI-DI
00810055522880 EUDAMED
Basic UDI-DI
081005552BluntPin3C EUDAMED
Direct Marketing DI
00810055522880 EUDAMED
EMDN Code
P091399 ORTHOPAEDIC IMPLANT INSTRUMENTS, SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

Blunt pin by Si-Bone Inc. — Class IIa — MDR — 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

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Manufacturer

Manufacturer
SI-BONE, Inc.
EUDAMED SRN
US-MF-000028624
Authorised Representative
ICON (LR) Limited IE-AR-000006507

Sources (1)

  • EUDAMED 4bf249c5-3337-4fc7-b456-d57ff45674f6 61 fields · synced Jun 19, 2026