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Colgate Sensitive Pro Relief

by Colgate-Palmolive Manufacturing (Poland) Sp. z o.o.

Ref PL05157A, PL05174A

Active European Union

CE MDD

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-8714789481418EE Basic UDI-DI Date18 Nov 2024RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Trade Name
Colgate Sensitive Pro Relief
Colgate Sensitive Pro Relief Repair & Prevent
Model / Reference
PL05157A, PL05174A
Primary DI / UDI-DI
D-8714789481418EE, D-8718951079328D6
Basic UDI-DI
B-8714789481418EE, B-8718951079328D6
EMDN Code
Q019008 Dentinal desensitisers
Device Class
Class IIa
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
PL-MF-000018645

Other devices from Colgate-Palmolive Manufacturing (Poland) Sp. z o.o.

See all devices from Colgate-Palmolive Manufacturing (Poland) Sp. z o.o. →

Properties

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No