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Absorbent Nonwoven Compress

EUDAMED

Class I (EU MDR)

Ref 8002

by Bestreat Safety & First Aid Solution Co., Ltd.

Identity

Trade Name
Absorbent Nonwoven Compress EUDAMED
Device Name
Sterile Absorbent Nonwoven Compress EUDAMED
Model / Reference
8002 EUDAMED

Identifiers

Primary DI / UDI-DI
06975706488022 EUDAMED
Basic UDI-DI
697570648110MW EUDAMED
EMDN Code
M0202030101 NON-WOVEN GAUZE PADS, WITHOUT X-RAY DETECTABLE THREAD, STERILE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

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

Absorbent Nonwoven Compress by Bestreat Safety & First Aid Solution Co., Ltd. — 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

EUDAMED SRN
CN-MF-000029564
Authorised Representative
MedPath GmbH DE-AR-000000087

Sources (1)

  • EUDAMED de66fc5c-9027-4efd-bce8-5fe700dbfabf 61 fields · synced Jun 18, 2026