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Dehp

by CB Healthcare Consulting GmbH 293 variants

Ref 9790954Model TF-232 (DEHP)

Dehp (9790954) is a Class I device made by CB Healthcare Consulting GmbH, registered in EUDAMED on 28 May 2026 (Basic UDI-DI 4062183232035R), 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4062183232035R Basic UDI-DI 14062183011498UDI-DIDate28 May 2026RegisteredStatusActive

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  • Withdrawn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
Latex Gloves
Model / reference
TF-232 (DEHP), 9790954
Primary DI / UDI-DI
14062183011498
Basic UDI-DI
4062183232035R
Unit of use DI
04062183011491
EMDN code
T010201 Latex examination / treatment gloves
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005902

Other devices from CB Healthcare Consulting GmbH

See all devices from CB Healthcare Consulting GmbH →

Properties

  • Contains latex
  • Reprocessed single-use device
Other properties (12, all answered No)