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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

3701172200089 — Class IIa MDR by EFFIK S.A.

MD Atlas
EFFIK S.A.

EUDAMED last updated this device on Oct 21, 2025

3701172200089

3701172290000925Y9

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: EFFIK S.A.
UDI-DI code: 03701172200089
Reference / catalog number: 3701172200089

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Manufacturer information

Organization name: EFFIK S.A.
SRN: FR-MF-000000606
Manufacturer status: Active

Critical warnings

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

CW010
Do not use in case of pregnancy

Market distribution

Primary placement in France; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 03701172200089
Basic UDI-DI: 3701172290000925Y9
Reference / catalog number: 3701172200089
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: Contenu du GynEffik Connect : Boitier de rangement et de charge - Sonde d'électrostimulation - Télécommande - Chargeur électrique - Cable d'alimentation reliant le boîtier et le chargeur électrique [FR]
Additional information URL: https://www.gyneffik.fr/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

U070199INTERNAL SYSTEMS FOR THE TREATMENT OF INCONTINENCE - OTHER

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

This device is not currently linked to any other device.

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.