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Kit

EUDAMED

Class I (EU MDR)

Ref RP-KT-1007Ref RP-KTEL-1009

by AA Sales Ltd

Identity

Device Name
Kit EUDAMED
Kit Elbow EUDAMED
Model / Reference
RP-KT-1007 EUDAMED
RP-KTEL-1009 EUDAMED

Identifiers

Primary DI / UDI-DI
05065024143091 EUDAMED
05065024143145 EUDAMED
Basic UDI-DI
5065024143RP-KTTG EUDAMED
5065024143RP-KTEL5U 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

Kit 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 98491992-8187-4108-a6d9-5ff186d3c3ac 61 fields · synced Jul 17, 2026
  • EUDAMED 5a6edf57-a7ae-4b10-976d-9f86d9c295eb 61 fields · synced May 18, 2026