Trachospray Kit

by Medspray Anesthesia B.V. 2 variants

Ref 5910K101EN

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number87213980265910K1QJ Basic UDI-DI 08721398026022UDI-DI	Date16 Mar 2026Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference: 5910K101EN

Primary DI / UDI-DI: 08721398026022
Basic UDI-DI: 87213980265910K1QJ
EMDN Code: R9099 Respiratory and anaesthesia devices - other

Device Class: Class IIa
Medical Purpose: Te gebruiken voor orale toediening van goedgekeurde stoffen, door middel van een combinatie van verstuiven en het inademen van een fijne nevel, om zo het slijmvlies van de mondholte en de keel van de patiënt te verdoven.

Manufacturer details

EUDAMED SRN: NL-PR-000048640

Other devices from Medspray Anesthesia B.V.

Nasal Atomiser Adapter

Class I
Trachospray Kit

Class IIa

Properties

Other properties (1)

Sterile: No