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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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Cryolipolysis Gel Pad — 3 UDI-DI variants, MDR (DELEO S.A.S.)

MD Atlas
DELEO S.A.S.

Data from EUDAMED, last updated May 19, 2026

Cryolipolysis Gel Pad

36657490004065E

3 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: DELEO S.A.S.

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UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01HQWJ5DKTWVFG55QBG4BTPMXA

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

CONTOUR CRYOPROTECTIVE GEL PAD03665749000468
CRISTAL CRYOPROTECTIVE GEL PAD LARGE03665749000437
CRISTAL CRYOPROTECTIVE GEL PAD SMALL03665749000451

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 36657490004065E
Device name: Cryolipolysis Gel Pad
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 1, 2024

Manufacturer & authorised representative

Manufacturer

Name: DELEO S.A.S.
SRN: FR-MF-000000215
Country: France
Email: qualite@deleo.fr
Phone: +33494458375

Variants by status