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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

3770023344 029 — Class I MDR by SATISFORM

MD Atlas
SATISFORM

EUDAMED last updated this device on Apr 9, 2026

3770023344 029

3770023344DPAMEDWN

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SATISFORM
UDI-DI code: 37700233440294
Reference / catalog number: 3770023344 029

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Manufacturer information

Organization name: SATISFORM
SRN: FR-MF-000002507
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Aug 26, 2019	Still on market

Device identification

Trade name: not provided
UDI-DI code: 37700233440294
Basic UDI-DI: 3770023344DPAMEDWN
Reference / catalog number: 3770023344 029
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: 1
Additional product description: Medical device for thoraco-lumbo-pelvic mobility and core muscles strengthening.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z120616ELECTROMECHANICAL SYSTEMS FOR PHYSICAL THERAPY

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.