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Himosta

EUDAMED

Class I (EU MDR)

Ref NP-ES15S

by Cenefom Corp.

Identity

Trade Name
HIMOSTA EUDAMED
Device Name
ENT Sponge EUDAMED
Model / Reference
NP-ES15S EUDAMED

Identifiers

Primary DI / UDI-DI
04711552923025 EUDAMED
Basic UDI-DI
471155292ENTHD EUDAMED
Direct Marketing DI
04711552923025 EUDAMED
EMDN Code
M040799 SPECIAL PADS - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain 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

Himosta by Cenefom Corp. — 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
Cenefom Corp.
EUDAMED SRN
TW-MF-000012190
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 7c15f92f-6e80-4bdf-83a6-853cdc1d3744 61 fields · synced Jun 19, 2026