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Embra® Nonwoven swabs 10 x 10 cm, non-sterile

EUDAMED

Class I (EU MDR)

Ref 2231953403

by OneMed Group Oy

Identity

Trade Name
Embra® Nonwoven swabs 10 x 10 cm, non-sterile EUDAMED
Device Name
Swabs Nonwoven, folded, non-sterile EUDAMED
Model / Reference
2231953403 EUDAMED

Identifiers

Primary DI / UDI-DI
06438129370270 EUDAMED
Basic UDI-DI
6438129B0011GX EUDAMED
EMDN Code
M0202010102 NON-WOVEN FOLDED GAUZES, WITHOUT X-RAY DETECTABLE THREAD, NON-STERILE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Sweden 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

Embra® Nonwoven swabs 10 x 10 cm, non-sterile by OneMed Group Oy — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
OneMed Group Oy
EUDAMED SRN
FI-MF-000000642

Sources (1)

  • EUDAMED 0a0df71b-d2f2-4398-9a6f-a8ab18508158 61 fields · synced Oct 6, 2026