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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

SRT55 - EUR — Class I MDR by DESSINTEY

MD Atlas
DESSINTEY

EUDAMED last updated this device on Feb 26, 2026

SRT55 - EUR

3770024593SRT555F

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: DESSINTEY
UDI-DI code: 03770024593358
Reference / catalog number: SRT55 - EUR

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Manufacturer information

Organization name: DESSINTEY
SRN: FR-MF-000009697
Manufacturer status: Active

Related devices

IVS3 - ESP3770024593IVS33BOn the market IVS3 - NORDIC3770024593IVS33BOn the market IVS3 - BEL3770024593IVS33BOn the market IVS3 - EUR3770024593IVS33BOn the market IVS33770024593IVS33BOn 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 Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement		Still on market
France		Still on market

Device identification

Trade name: not provided
UDI-DI code: 03770024593358
Basic UDI-DI: 3770024593SRT555F
Reference / catalog number: SRT55 - EUR
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: Self-Rehabilitation Technology (upper limbs)
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y0504ARMS, TORSO AND LEGS RE-EDUCATION DEVICES

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