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Manual Resuscitator

EUDAMED

Class IIa (EU MDR)

Ref SMRA03SModel Silicone

by Ningbo Luke Medical Devices Co., LTD

Identity

Device Name
Manual Resuscitator EUDAMED
Model / Reference
Silicone EUDAMED
SMRA03S EUDAMED

Identifiers

Primary DI / UDI-DI
06970240894209 EUDAMED
Basic UDI-DI
697024089MRYR EUDAMED
Direct Marketing DI
06970240894209 EUDAMED
EMDN Code
R03020201 MANUALLY OPERATED PULMONARY RESUSCITATORS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Romania 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 resuscitator, manual, single-use

Manual Resuscitator by Ningbo Luke Medical Devices Co., LTD — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Pulmonary resuscitator, manual, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000011732
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 56d426c9-0474-4a90-91fc-61db9bde536b 61 fields · synced Jun 11, 2026