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Flexible Guide Pin for Arthrex® Flexible Reamer

EUDAMED

Class IIa (EU MDR)

Ref 109120s0arModel Cruciate Ligament Instruments

by T.A.G. Medical products corporation LTD.

Identity

Trade Name
Flexible Guide Pin for Arthrex® Flexible Reamer EUDAMED
Device Name
Cruciate Ligament Instruments EUDAMED
Model / Reference
Cruciate Ligament Instruments EUDAMED
109120s0ar EUDAMED

Identifiers

Primary DI / UDI-DI
10810190018788 EUDAMED
Basic UDI-DI
81012846CRUCIAETLIGINSV3 EUDAMED
Direct Marketing DI
10810190018788 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

Flexible Guide Pin for Arthrex® Flexible Reamer by T.A.G. Medical products corporation LTD. — 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

EUDAMED SRN
IL-MF-000029151
Authorised Representative
MedNet EC-REP IIb GmbH DE-AR-000011192

Sources (1)

  • EUDAMED d5c5c544-1882-44b5-8d1a-03189936a710 61 fields · synced Jun 18, 2026