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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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Cevidra cream for nuclear… — 2 UDI-DI variants, MDR

MD Atlas
Laboratoire CEVIDRA

Data from EUDAMED, last updated May 19, 2026

Cevidra cream for nuclear decontamination

3664831DM02CEVIDRANJ

2 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 CEVIDRA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3664831DM02CEVIDRANJ
Device name: Cevidra cream for nuclear decontamination
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 5, 2021

Manufacturer & authorised representative

Manufacturer

Name: Laboratoire CEVIDRA
SRN: FR-MF-000011081
Country: France
Email: p.chanton@cevidra.com
Phone: 0493705831

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01FKR8G2CKZ7JZGD64F0GAWE7R

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

Cevidra cream for nuclear decontamination03664831000126
Cevidra cream for nuclear decontamination03664831000096