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Laerdal Silicone Resuscitators

EUDAMED

Class IIa (EU MDR)

Ref 85005000Model Laerdal Silicone Resuscitator

by Laerdal Medical AS

Identity

Trade Name
Laerdal Silicone Resuscitators EUDAMED
Device Name
Laerdal Silicone Resuscitator EUDAMED
Model / Reference
Laerdal Silicone Resuscitator EUDAMED
85005000 EUDAMED

Identifiers

Primary DI / UDI-DI
07045430044753 EUDAMED
Basic UDI-DI
0704543209945T6 EUDAMED
Direct Marketing DI
07045430044753 EUDAMED
EMDN Code
R03020199 VENTILATION BALLOONS - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Norway 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

Laerdal Silicone Resuscitators by Laerdal Medical AS — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Laerdal Medical AS
EUDAMED SRN
NO-MF-000000012

Sources (1)

  • EUDAMED 4b196fc0-44b8-4441-b8d6-5d5dcb134f7a 61 fields · synced Jun 18, 2026