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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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Cale dent — 10 UDI-DI variants, MDR (MV2G INTERNATIONAL)

MD Atlas
MV2G INTERNATIONAL

Data from EUDAMED, last updated May 19, 2026

Cale dent

376011451BBNZ

10 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: MV2G INTERNATIONAL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 376011451BBNZ
Device name: Cale dent
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 6, 2026

Manufacturer & authorised representative

Manufacturer

Name: MV2G INTERNATIONAL
SRN: FR-MF-000020643
Country: France
Email: information@tec-care.com
Phone: +33 3 72 73 63 20

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01KQYMKYNWP6ZZZF5XWQDA8P13

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

ENCD04-WS03760114510044
ENCDOXY-WS03760114510068
ENCDOXY03760114510051
ENCD01S03760114510082
ENCD03T03760114510105
ENCD03-WS03760114510020
ENCD03R03760114510099
ENCD0303760114510013
ENCD0403760114510037
ENCD0103760114510075