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AMSure® Mucus Trap

EUDAMED

Class I (EU MDR)

Ref AS79400

by Amsino International Inc.

Identity

Trade Name
AMSure® Mucus Trap EUDAMED
Device Name
Mucus Trap EUDAMED
Model / Reference
AS79400 EUDAMED

Identifiers

Primary DI / UDI-DI
10704411021612 EUDAMED
Basic UDI-DI
B-10704411021612 EUDAMED
EMDN Code
W05019003 SPUTUM COLLECTION DEVICES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

AMSure® Mucus Trap by Amsino International, Inc. — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
US-MF-000007234
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 19982594-aa94-4a3c-92d9-5b489c08d2e3 61 fields · synced Jul 9, 2026