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Humidifier

EUDAMED

Class I (EU MDR)

Ref RP-HD-1108Ref RP-HD-1118

by AA Sales Ltd

Identity

Device Name
Humidifier EUDAMED
Model / Reference
RP-HD-1108 EUDAMED
RP-HD-1118 EUDAMED

Identifiers

Primary DI / UDI-DI
05065024143138 EUDAMED
05065024143121 EUDAMED
Basic UDI-DI
5065024143RP-HDS7 EUDAMED
EMDN Code
R03010180 ARTIFICIAL VENTILATION MASKS - ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Northern Ireland 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

Humidifier by AA Sales Ltd — 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
AA Sales Ltd
EUDAMED SRN
UK-MF-000047880
Authorised Representative
Share info GmbH DE-AR-000005132

Sources (2)

  • EUDAMED ca34b339-a3a0-497c-82bb-fb3daef7999f 61 fields · synced Jul 13, 2026
  • EUDAMED 981f7cde-1a8e-4e46-baf3-87eb8a1e30ea 61 fields · synced May 17, 2026