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Endoragard

EUDAMED

Class I (EU MDR)

Ref 29520DX

by Kerr Italia Srl

Identity

Trade Name
Endoragard EUDAMED
Device Name
Endoragard EUDAMED
Model / Reference
29520DX EUDAMED

Identifiers

Primary DI / UDI-DI
08055165097831 EUDAMED
Basic UDI-DI
80515118710001195J EUDAMED
EMDN Code
R9099 RESPIRATORY AND ANAESTHESIA DEVICES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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

Category: Pulmonary function analysis system, adult

Endoragard by Kerr Italia Srl — 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

Manufacturer
Kerr Italia Srl
EUDAMED SRN
IT-MF-000007768

Sources (1)

  • EUDAMED 45a3f305-e27c-4566-94a6-113b88ef32c0 61 fields · synced Jul 9, 2026