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Kosmos Torso NXT

by EchoNous

Part of a family of 31 devices: see the family page

Ref P009076

Kosmos Torso NXT (P009076) is a Class IIa device made by EchoNous, registered in EUDAMED on 29 Oct 2021 (Basic UDI-DI 93532780KOSMOSWH), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number93532780KOSMOSWH Basic UDI-DI 09353278001059UDI-DIDate29 Oct 2021RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Kosmos
Model / reference
P009076
Primary DI / UDI-DI
09353278001059
Basic UDI-DI
93532780KOSMOSWH
EMDN code
Z110402010301 Transcutaneous ultrasound sector probes (phased array), two–dimensional
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Denmark

Manufacturer details

EUDAMED SRN
US-MF-000004161
Authorised representative
Advena Limited MT-AR-000000234

Similar devices in this category

Other devices filed under TRANSCUTANEOUS ULTRASOUND SECTOR PROBES (PHASED ARRAY), TWO–DIMENSIONAL.

Other devices from EchoNous

See all devices from EchoNous →

Properties

Other properties (14, all answered No)