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Momosan

EUDAMED

Class IIb (EU MDR)

Ref 61901S

by Moltoplast GmbH

Identity

Trade Name
Momosan EUDAMED
Device Name
MOMOSAN-weiss steril EUDAMED
Model / Reference
61901S EUDAMED

Identifiers

Primary DI / UDI-DI
90060180090126 EUDAMED
Basic UDI-DI
90060186100075 EUDAMED
Direct Marketing DI
90060180090126 EUDAMED
EMDN Code
M04040601 POLYURETHANE DRESSINGS, NON-COMBINED EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Austria 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

Category: Negative-pressure wound therapy system foam dressing, non-antimicrobial

Momosan by Moltoplast GmbH — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Negative-pressure wound therapy system foam dressing, non-antimicrobial.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Moltoplast GmbH
EUDAMED SRN
AT-MF-000004503

Sources (1)

  • EUDAMED f5c2f937-b810-4c49-b1f5-3984c85aa2d0 61 fields · synced Jun 18, 2026