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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

PAD0113 — Class I MDR by MV2G INTERNATIONAL

MD Atlas
MV2G INTERNATIONAL

EUDAMED last updated this device on May 6, 2026

PAD0113

376011451PADE9

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MV2G INTERNATIONAL
UDI-DI code: 03760114518248
Reference / catalog number: PAD0113

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Manufacturer information

Organization name: MV2G INTERNATIONAL
SRN: FR-MF-000020643
Manufacturer status: Active

Related devices

ENRKIT07-200376011451CBUDDOn the market ENRKIT13376011451CBUDDOn the market ENR04-200Y376011451CBUDDOn the market ENRKIT05-200Y376011451CBUDDOn the market ENRKIT2-05-230376011451CBUDDOn 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

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 03760114518248
Basic UDI-DI: 376011451PADE9
Reference / catalog number: PAD0113
Issuing entity: GS1

Classification

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

Device details

Quantity: 500
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

S9080DEVICES FOR STERILISATION (EXCLUDING CAT. D - Z) - 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
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Software identification