← Back to catalogue

Respiratory Humidification Systems

EUDAMED

Class IIa (EU MDR)

Ref HUMID-A

by Shenyang RMS Medical Tech Co., Ltd.

Identity

Device Name
Respiratory Humidification Systems EUDAMED
Model / Reference
HUMID-A EUDAMED

Identifiers

Primary DI / UDI-DI
06957469401883 EUDAMED
Basic UDI-DI
6957469402002DS EUDAMED
EMDN Code
R040201 TRACHEOSTOMY HUMIDIFIERS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

Respiratory Humidification Systems by Shenyang RMS Medical Tech Co., Ltd. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000023286
Authorised Representative
MedPath GmbH DE-AR-000000087

Sources (1)

  • EUDAMED 8b941996-e503-478d-86e8-d593df05fd46 61 fields · synced Jun 18, 2026