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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Colgate Sensitive Pro Relief Whitening — 1 UDI-DI variant, MDD

MD Atlas
Colgate-Palmolive Manufacturing (Poland) sp. z o.o.

Data from EUDAMED, last updated May 30, 2026

Colgate Sensitive Pro Relief Whitening

B-8714789529561EP

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIa

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: Colgate-Palmolive Manufacturing (Poland) sp. z o.o.

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: D1366300020
Type: refdata.legacy.mdd-certificate-type.v
Notified body: mdc medical device certification GmbH (0483)
Validity: Jan 21, 2024

Identity & classification

Basic UDI-DI: B-8714789529561EP
Device name: Colgate Sensitive Pro Relief Whitening
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: Nov 18, 2024

Manufacturer & authorised representative

Manufacturer

Name: Colgate-Palmolive Manufacturing (Poland) sp. z o.o.
SRN: PL-MF-000018645
Country: Poland
Email: meddev_man@colpal.com
Phone: +48 74 856 7000

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01JCZKMS1NKYQ1DXNQ8JX2P30G

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

Colgate Sensitive Pro Relief WhiteningD-8714789529561EP