← Back to catalogue

Comprese netesut(EVRIKA)

EUDAMED

Class I (EU MDR)

Ref RMNY5X5X4P20SNS

by Jiangsu Feixia Medical Products Co., Ltd

Identity

Trade Name
Comprese netesut(EVRIKA) EUDAMED
Device Name
Non-woven Sponge EUDAMED
Model / Reference
RMNY5X5X4P20SNS EUDAMED

Identifiers

Primary DI / UDI-DI
06970101555409 EUDAMED
Basic UDI-DI
697010155NWS001DD EUDAMED
Unit of Use DI
86970101555405 EUDAMED
EMDN Code
M0202010101 NON-WOVEN FOLDED GAUZES, WITHOUT X-RAY DETECTABLE THREAD, STERILE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Romania 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

Comprese netesut(EVRIKA) by Jiangsu Feixia Medical Products 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

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

Manufacturer

EUDAMED SRN
CN-MF-000016183
Authorised Representative
MedPath GmbH DE-AR-000000087

Sources (1)

  • EUDAMED 24358e25-859e-4d36-a1bd-26808b737272 61 fields · synced Jun 19, 2026