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Arthrex BioXpress

EUDAMED

Class IIa (EU MDR)

Ref ABS-10053-10

by Micromedics, Inc.

Identity

Trade Name
Arthrex BioXpress EUDAMED
Device Name
Graft Delivery Device EUDAMED
Model / Reference
ABS-10053-10 EUDAMED

Identifiers

Primary DI / UDI-DI
20815634020331 EUDAMED
Basic UDI-DI
B-20815634020331 EUDAMED
EMDN Code
A020199 SYRINGES, SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

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

Arthrex BioXpress by Micromedics, Inc. — Class IIa — 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
Micromedics, Inc.
EUDAMED SRN
US-MF-000018365
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (1)

  • EUDAMED 07ad9d54-b1a8-4679-8a40-e39b3271c930 61 fields · synced Jun 19, 2026