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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

NephroWise — Class IIa MDR by SÊMEIA

MD Atlas
SÊMEIA

EUDAMED last updated this device on Feb 7, 2025

NephroWise

3760361030188N

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SÊMEIA
UDI-DI code: 37603610301808
Reference / catalog number: MedicWise

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Manufacturer information

Organization name: SÊMEIA
SRN: FR-MF-000018486
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Feb 7, 2025	Still on market

Device identification

Trade name: NephroWise
UDI-DI code: 37603610301808
Basic UDI-DI: 3760361030188N
Reference / catalog number: MedicWise
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: https://www.notion.so/semeia/Manuels-utilisateurs-S-meia-Wise-V7-14-0-21e890468ac64dd2a20916811b44b5f9
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z129092VARIOUS INSTRUMENTS FOR FUNCTIONAL EXPLORATION AND THERAPEUTIC INTERVENTIONS - 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

MedicWiseB-37603610302584On the market MedicWise3760361030198QOn the market MedicWiseB-37603610302416On the market MedicWiseB-37603610302102On the market MedicWise37603610302089On 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.