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Comepa

by Telic, S.A.U. 3 variants

Part of a family of 36 devices: see the family page

Ref 3G250US

Comepa (3G250US) is a Class I device made by Telic, S.A.U., registered in EUDAMED on 9 Aug 2024 (Basic UDI-DI 8427734USGEL8L), 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8427734USGEL8L Basic UDI-DI 03663996018762UDI-DIDate9 Aug 2024RegisteredStatusActive

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  • Withdrawn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

Device name
Ultrasound gels
Model / reference
3G250US
Primary DI / UDI-DI
03663996018762
Basic UDI-DI
8427734USGEL8L
EMDN code
Z11040185 Ultrasound scanners - consumables
Device class
Class I
EU registration type
Standard device
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000001853

Similar devices in this category

Other devices filed under ULTRASOUND SCANNERS - CONSUMABLES.

Other devices from Telic, S.A.U.

See all devices from Telic, S.A.U. →

Properties

Other properties (14, all answered No)