← Back to catalogue

Muslera AIRTEX

EUDAMED

Class I (EU MDR)

Ref OST247Ref ATXOS901

by Prim, S.a.

Identity

Trade Name
Muslera AIRTEX EUDAMED
Muslera AIRTEX OS EUDAMED
Device Name
Ortesis Femorales EUDAMED
Model / Reference
OST247 EUDAMED
ATXOS901 EUDAMED

Identifiers

Primary DI / UDI-DI
08434048030224 EUDAMED
08434048418473 EUDAMED
Basic UDI-DI
843404825ORTESISMUSLO44 EUDAMED
EMDN Code
Y061217 THIGH ORTHOSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

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

Muslera AIRTEX by Prim S.a. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Prim, S.a.
EUDAMED SRN
ES-MF-000004651

Sources (2)

  • EUDAMED 28211788-4443-4149-a221-121699399908 61 fields · synced Jul 26, 2026
  • EUDAMED 8184cdda-6d70-4d40-a546-484175fc0586 61 fields · synced May 19, 2026