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GuidingArm f/PE-Inlay le

EUDAMED

Class I (EU MDR)

Ref PDL652Model Reusable instrumentation

by Centinel Spine, LLC

Identity

Trade Name
GuidingArm f/PE-Inlay le EUDAMED
Model / Reference
Reusable instrumentation EUDAMED
PDL652 EUDAMED

Identifiers

Primary DI / UDI-DI
00843193119599 EUDAMED
Basic UDI-DI
08431931InstrumentsU5 EUDAMED
EMDN Code
L091104 ORTHOPAEDIC PROSTHESES POSITIONERS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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: Orthopaedic implant impactor, reusable

GuidingArm f/PE-Inlay le by Centinel Spine, LLC — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implant impactor, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Centinel Spine, LLC
EUDAMED SRN
US-MF-000013245
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED f99c947a-843d-4e12-98ed-6c0c8b9f070b 61 fields · synced Jun 18, 2026