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Woson

by Ningbo Jiangbei Woson Medical Instrument Co., Ltd. 14 variants

Ref ARIES

Woson (ARIES) is a Class IIa device made by Ningbo Jiangbei Woson Medical Instrument Co., Ltd., registered in EUDAMED on 8 Jul 2026 (Basic UDI-DI 697124689SSJFSM), active as of 23 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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697124689SSJFSM Basic UDI-DI 06971246891056UDI-DIDate8 Jul 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Steam Sterilizer
Model / reference
ARIES
Primary DI / UDI-DI
06971246891056
Basic UDI-DI
697124689SSJFSM
Direct marketing DI
06971246891056
EMDN code
Z12011305 Small load autoclaves with a chamber smaller than 1 standard sterilisation unit
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Romania

Manufacturer details

EUDAMED SRN
CN-MF-000035366
Authorised representative
Caretechion GmbH DE-AR-000005946

Similar devices in this category

Other devices filed under SMALL LOAD AUTOCLAVES WITH A CHAMBER SMALLER THAN 1 STANDARD STERILISATION UNIT.

Other devices from Ningbo Jiangbei Woson Medical Instrument Co., Ltd.

See all devices from Ningbo Jiangbei Woson Medical Instrument Co., Ltd. →

Properties

Other properties (14, all answered No)