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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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Organization name
UDI-DI code
Reference / catalog number

MVB2EOS002 — Class IIb MDR by Cavagna Group S.p.A.

MD Atlas
Cavagna Group S.p.A.

EUDAMED last updated this device on May 13, 2026

MVB2EOS002

08500211332GB

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Cavagna Group S.p.A.
UDI-DI code: 00850049890205
Reference / catalog number: MVB2EOS002

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View device family (Basic UDI)

Manufacturer information

Organization name: Cavagna Group S.p.A.
SRN: IT-MF-000028356
Manufacturer status: Active

Related devices

MVA2EOS03108500211332GBOn the market MVA2UOS07008500211332GBOn the market MVA2EOS02008500211332GBOn the market MVA2EOS04408500211332GBOn the market MVA2EOS08908500211333GDOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Critical warnings

6 warnings recorded — scroll inside the panel to see all entries.

CW026
EUDAMED did not publish a description for this code.
CW030
EUDAMED did not publish a description for this code.
CW276
EUDAMED did not publish a description for this code.
CW094
EUDAMED did not publish a description for this code.
CW096
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Apr 15, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 00850049890205
Basic UDI-DI: 08500211332GB
Reference / catalog number: MVB2EOS002
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: https://www.cavagnagroup.com/
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)00850049890205

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Z120309MEDICAL/MEDICINAL GAS PIPELINE SYSTEMS AND RELATED ACCESSORIES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

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