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AeroChamber Plus*

EUDAMED

Class I (EU MDR)

Ref 101502

by Trudell Medical International

Identity

Trade Name
AeroChamber Plus* EUDAMED
Device Name
Valved Holding Chamber EUDAMED
Model / Reference
101502 EUDAMED

Identifiers

Primary DI / UDI-DI
00762860291065 EUDAMED
Basic UDI-DI
762860VHC1NL EUDAMED
EMDN Code
R9099 RESPIRATORY AND ANAESTHESIA DEVICES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Pulmonary function analysis system, adult

AeroChamber Plus* by Trudell Medical International — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Pulmonary function analysis system, adult.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CA-MF-000009860
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 8b5f6101-167f-4b12-bcd6-cdc985dc8d78 61 fields · synced May 23, 2026