← Back to catalogue

nasal aspirator

EUDAMED

Class I (EU MDR)

Ref ASPIModel ASPI,ASPI2,ASPI3,ASPI-VRef ASPI-VRef ASPI 2

by Cotronic Technology Ltd

Identity

Device Name
nasal aspirator EUDAMED
Model / Reference
ASPI,ASPI2,ASPI3,ASPI-V EUDAMED
ASPI EUDAMED
ASPI-V EUDAMED
ASPI 2 EUDAMED

Identifiers

Primary DI / UDI-DI
06933345720002 EUDAMED
06933345720101 EUDAMED
06933345720026 EUDAMED
Basic UDI-DI
69333457nasalaspiratorYP EUDAMED
Direct Marketing DI
06933345720026 EUDAMED
EMDN Code
R05010399 MUCOSITY ASPIRATORS - OTHER 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

nasal aspirator by Cotronic Technology 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

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

Manufacturer

EUDAMED SRN
CN-MF-000023700
Authorised Representative
Share info GmbH DE-AR-000005132

Sources (3)

  • EUDAMED b22582ec-0485-4cfb-aa69-0dd01f410750 61 fields · synced Jul 25, 2026
  • EUDAMED a8436c28-d62b-4041-8d1e-abdb8755a7cf 61 fields · synced May 18, 2026
  • EUDAMED c678dfe2-bfda-494d-9018-26c4d6c70c90 61 fields · synced Jul 25, 2026