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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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CARVI — 3 UDI-DI variants, MDR (BMB MEDICAL)

MD Atlas
BMB MEDICAL

Data from EUDAMED, last updated May 19, 2026

CARVI

376034596CRCO6BS

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: BMB MEDICAL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 376034596CRCO6BS
Device name: CARVI
Device model: CARVI
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 8, 2024

Manufacturer & authorised representative

Manufacturer

Name: BMB MEDICAL
SRN: FR-MF-000011270
Country: France
Email: qualite@hacare.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01HP41H7VDYEX67AEYY197P8M7

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

CARVI 60CM37603459603354
CARVI 70CM37603459603422
CARVI 80CM37603459603590