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Non woven Swabs

EUDAMED

Class I (EU MDR)

Ref 3900

by CliniMed Limited

Identity

Trade Name
Non woven Swabs EUDAMED
Device Name
Non-woven Swabs EUDAMED
Model / Reference
3900 EUDAMED

Identifiers

Primary DI / UDI-DI
05017950012026 EUDAMED
Basic UDI-DI
050179500NonWovenSwabsY6 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
Ireland 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

Non woven Swabs by CliniMed Limited — 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
CliniMed Limited
EUDAMED SRN
GB-MF-000023784
Authorised Representative
Advena Limited MT-AR-000000234

Sources (1)

  • EUDAMED 0516e567-2860-4268-b8ce-2e9a5a8897a5 61 fields · synced Jun 19, 2026