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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

Resilience PRO V3 — Class IIa MDR by Resilience MD

MD Atlas
Resilience MD

EUDAMED last updated this device on Mar 7, 2024

Resilience PRO V3

376035694OncolaxyV37P

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Resilience MD
UDI-DI code: 03760356940005
Reference / catalog number: Resilience PRO V3

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Manufacturer information

Organization name: Resilience MD
SRN: FR-MF-000000678
Manufacturer status: Active

Market distribution

Primary placement in France; available across 2 countries total.

Country	On market since	Until
FrancePrimary placement	Dec 16, 2021	Still on market
Belgium	Feb 27, 2024	Still on market

Device identification

Trade name: Resilience PRO V3
UDI-DI code: 03760356940005
Basic UDI-DI: 376035694OncolaxyV37P
Reference / catalog number: Resilience PRO V3
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
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)

Z12040192GENERAL MEDICINE DIAGNOSIS AND MONITORING INSTRUMENTS - MEDICAL DEVICE SOFTWARE

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
Serial number
Software identification

Related devices

EDRA PRO376035694EdraproR3On the market 3760356940012376035694ResilienceproYFOn the market GutyCare V2376035694GutyCareU4On 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.