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2-in-1 Muffled Adapter

EUDAMED

Class I (EU MDR)

Ref R219P50

by Maxtec, LLC

Identity

Trade Name
2-in-1 Muffled Adapter EUDAMED
Device Name
2-in-1 Muffled Adapter EUDAMED
Model / Reference
R219P50 EUDAMED

Identifiers

Primary DI / UDI-DI
00817770020776 EUDAMED
Basic UDI-DI
0817770022IN1ADAPTERHJ EUDAMED
Direct Marketing DI
00817770020776 EUDAMED
EMDN Code
A070199 ADAPTERS AND CONNECTORS - OTHER 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

2-in-1 Muffled Adapter by Maxtec, 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

Manufacturer
Maxtec, LLC
EUDAMED SRN
US-MF-000003961
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 3218a65b-5791-40fc-be15-95863edf19dd 61 fields · synced Jul 9, 2026