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Aquavap

by Sterlab 2 variants

Ref 412, 422Model AQUAVAP

Aquavap (412) is a Class I device made by Sterlab, registered in EUDAMED on 24 Apr 2025 (Basic UDI-DI 376031457AQUAVAPK7), active as of 22 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number376031457AQUAVAPK7 Basic UDI-DI Date24 Apr 2025RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
AQUAVAP, 412, 422
Primary DI / UDI-DI
03760314570619, 03760314570602
Basic UDI-DI
376031457AQUAVAPK7
EMDN code
S9080 Devices for sterilisation (excluding cat. d - z) - accessories
Device class
Class I
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000001369

Related devices

Category: Sterilizer/disinfector rack

Similar devices in this category

Other devices filed under DEVICES FOR STERILISATION (EXCLUDING CAT. D - Z) - ACCESSORIES.

Other devices from Sterlab

See all devices from Sterlab →

Properties

Other properties (14, all answered No)