← Back to catalogue

Supramid Aragó

EUDAMED

Class IIb (EU MDR)

Ref 26011

by Laboratorio Aragó S.L.

Identity

Trade Name
Supramid Aragó EUDAMED
Device Name
Supramid Aragó EUDAMED
Model / Reference
26011 EUDAMED

Identifiers

Primary DI / UDI-DI
08427599023548 EUDAMED
Basic UDI-DI
8427599DTTF0247F EUDAMED
EMDN Code
H010201020101 POLYAMIDE MULTIFILAMENT WITH NEEDLE EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Sutures

Yes

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

Supramid Aragó by Laboratorio Aragó S.L. — Class IIb — 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

EUDAMED SRN
ES-MF-000001958

Sources (1)

  • EUDAMED 6b1501c9-56bc-44f7-b2d3-f30352d5119f 61 fields · synced Oct 6, 2026