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nCannula, #0 w/nBonnet

EUDAMED

Class IIa (EU MDR)

Ref AN0020Model (G) Bubble CPAP SystemRef AN0075

by GaleMed Corporation

Identity

Trade Name
nCannula, #0 w/nBonnet EUDAMED
nCannula Kit, #0 w/nBonnet EUDAMED
Device Name
nCannula Kit EUDAMED
Model / Reference
(G) Bubble CPAP System EUDAMED
AN0020 EUDAMED
AN0075 EUDAMED

Identifiers

Primary DI / UDI-DI
04710810106040 EUDAMED
04710810103872 EUDAMED
Basic UDI-DI
471081008NNGN95 EUDAMED
EMDN Code
R02010401 CPAP CIRCUITS EUDAMED

Classification

Device Class
Class IIa 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

nCannula, #0 w/nBonnet by GaleMed Corporation — Class IIa — 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
GaleMed Corporation
EUDAMED SRN
TW-MF-000022411
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED bc68b11a-c2cd-463a-99fd-e00722f83b75 61 fields · synced Aug 3, 2026
  • EUDAMED 79612c25-ac71-4687-be43-1ba4f84e74f5 61 fields · synced May 18, 2026