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Manual Resuscitator

EUDAMED

Class IIa (EU MDR)

Ref PA40623112Model SEBS

by Hangzhou Formed Medical Devices Co., Ltd.

Identity

Trade Name
Manual Resuscitator EUDAMED
Device Name
Manual Resuscitator EUDAMED
Model / Reference
SEBS EUDAMED
PA40623112 EUDAMED

Identifiers

Primary DI / UDI-DI
06923310909679 EUDAMED
Basic UDI-DI
69233109PA40629C EUDAMED
EMDN Code
R03020201 MANUALLY OPERATED PULMONARY RESUSCITATORS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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 Hangzhou Formed 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-000011212
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 6b3beaf1-97fc-445b-8e7e-cb17cb51a5c0 61 fields · synced Jun 18, 2026