Portable Mesh Nebulizer

by Shenzhen Jermei Medical Device Technology Co., Ltd. 17 variants

Ref /Model JM802,JM810, JM811,JM817, JM818,JM821,JM822,JM827, JM828,JM829, JM830,JM832,JM833, JM835,JM836, JM837, JM838,JM839, JM841, JM842,JM843,JM888

Active European Union

CE MDR

Valid until

5 May 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier SGS FIMKO OY

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number697243381JM821EQ Basic UDI-DI 06972433810119UDI-DI	Date15 May 2026Registered	StatusActive
European Union	CE/MDR	NumberFI26/1008024	Date6 May 2026Issued	StatusActive expires 5 May 2031

Certificates

1 certificate · EUDAMED

FI26/1008024 Active

Quality management system EU MDR

Certifier

SGS FIMKO OY 0598

Issued
6 May 2026

Expires
5 May 2031

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference: JM802, JM810, JM811, JM817, JM818, JM821, JM822, JM827, JM828, JM829, JM830, JM832, JM833, JM835, JM836, JM837, JM838, JM839, JM841, JM842, JM843, JM888, /

Primary DI / UDI-DI: 06972433810119
Basic UDI-DI: 697243381JM821EQ
Direct Marketing DI: 06972433810119
EMDN Code: Z12040210 Ultrasonic nebulisers

Device Class: Class IIa
EU market of registration: Germany

Manufacturer details

EUDAMED SRN: CN-MF-000039164
Authorised representative: Luxus Lebenswelt GmbH DE-AR-000005110

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Properties

Other properties (13)