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Silicone Manual Resuscitator

EUDAMED

Class IIa (EU MDR)

Ref EMR0101011Model Adult, Pediatric, Infant,LSIA-001/RTMA4,LSIA-002/RTMA4

by Xiamen Compower Medical Tech. Co., Ltd.

Identity

Trade Name
Silicone Manual Resuscitator EUDAMED
Device Name
Silicone Manual Resuscitator EUDAMED
Model / Reference
Adult, Pediatric, Infant,LSIA-001/RTMA4,LSIA-002/RTMA4 EUDAMED
EMR0101011 EUDAMED

Identifiers

Primary DI / UDI-DI
06946430422668 EUDAMED
Basic UDI-DI
694643041759101QY EUDAMED
Direct Marketing DI
06946430422668 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

Silicone Manual Resuscitator by Xiamen Compower Medical Tech. 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-000011703
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 78b1b567-2143-4d73-838a-5fef4bd78a4a 61 fields · synced Jun 18, 2026