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Power-Drool

EUDAMED

Class IIa (EU MDR)

Ref SH-2082S

by Romsons Group Private Limited

Identity

Trade Name
POWER-DROOL EUDAMED
Device Name
NEBULIZER: Mask / Mouth Piece with Nebulization Chamber and Tubing. EUDAMED
Model / Reference
SH-2082S EUDAMED

Identifiers

Primary DI / UDI-DI
08907265208214 EUDAMED
Basic UDI-DI
8907265B019YV EUDAMED
EMDN Code
R03010304 AEROSOL THERAPY KITS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

Yes

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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Power-Drool by Romsons Group Private Limited — 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

EUDAMED SRN
IN-MF-000036506
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 7cc7f5eb-98a3-47fd-9b75-2e7804145baa 61 fields · synced Jun 19, 2026