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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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NOCICEPTOL GEL ANTI-DOULEUR — 5 UDI-DI variants, MDR

MD Atlas
LABORATOIRE POLIDIS

Data from EUDAMED, last updated May 19, 2026

NOCICEPTOL GEL ANTI-DOULEUR

3664538ADGL01NLQB

5 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: LABORATOIRE POLIDIS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3664538ADGL01NLQB
Device name: NOCICEPTOL GEL ANTI-DOULEUR
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 22, 2024

Manufacturer & authorised representative

Manufacturer

Name: LABORATOIRE POLIDIS
SRN: FR-MF-000004550
Country: France
Email: contact@polidis.fr

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01J5WMFP9Z50SPVEJRG83MHV7Y

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

NOCICEPTOL® GEL ANTI-DOULEUR03664538000061
NOCICEPTOL® GEL ANTI-DOULEUR03664538000146
NOCICEPTOL® GEL ANTI-DOULEUR03664538000139
581408403664538000504
581409003664538000511