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A2l®

EUDAMED

Class III (EU MDR)

Ref A2L9-9

by Eurospine Sarl

Identity

Trade Name
A2L® EUDAMED
Device Name
A2L Anterior Lumbar intervertebral fusion cage, non-sterile EUDAMED
Model / Reference
A2L9-9 EUDAMED

Identifiers

Primary DI / UDI-DI
A2L991 EUDAMED
Basic UDI-DI
B-A2L991 EUDAMED
EMDN Code
P09070101 SPINAL CAGES EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

A2l® by Eurospine Sarl — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Eurospine Sarl
EUDAMED SRN
FR-MF-000001820

Sources (1)

  • EUDAMED 44dcf51f-091d-43b0-a5cd-191d41819099 61 fields · synced Jun 18, 2026