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Receptal Ⓡ Kit

EUDAMED

Class I (EU MDR)

Ref 0G902K826M

by Amsino International Inc.

Identity

Trade Name
Receptal Ⓡ Kit EUDAMED
Device Name
Receptal kit EUDAMED
Model / Reference
0G902K826M EUDAMED

Identifiers

Primary DI / UDI-DI
10704411020226 EUDAMED
Basic UDI-DI
0704411462Z7 EUDAMED
EMDN Code
A06030401 INTRAOPERATIVE SUCTION CONTAINERS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands 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

Receptal Ⓡ Kit by Amsino International, Inc. — 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
US-MF-000007234
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED fc65e8a3-658e-4c93-b51b-078abf353895 61 fields · synced Jul 11, 2026