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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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CALECHE — 7 UDI-DI variants, MDR (France Reval)

MD Atlas
France Reval

Data from EUDAMED, last updated May 19, 2026

CALECHE

3666401BA005HT

7 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: France Reval

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3666401BA005HT
Device name: CALECHE
Device model: CALECHE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 12, 2026

Manufacturer & authorised representative

Manufacturer

Name: France Reval
SRN: FR-MF-000011523
Country: France
Email: responsablequalite@france-reval.com
Phone: +33 5 46 42 04 16

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01KKGS94XZKD544SBP7ZA15QEY

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

CALECHE36664010022886
CALECHE36664010023180
CALECHE36664010022954
CALECHE36664010022640
CALECHE36664010023012
CALECHE36664010023258
CALECHE COMPACT36664010022404