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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

EW1-RS1 — Class I MDR by Emovo Care

MD Atlas
Emovo Care

EUDAMED last updated this device on Apr 30, 2026

EW1-RS1

7649995625EW1QG

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Emovo Care
UDI-DI code: 07649995625046
Reference / catalog number: EW1-RS1

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Manufacturer information

Organization name: Emovo Care
SRN: CH-MF-000049487
Manufacturer status: Active

Related devices

Emovo Clinic7649995625EC1NLOn the market EW1-LL17649995625EW1QGOn the market EW1-LM17649995625EW1QGOn the market EW1-LS17649995625EW1QGOn the market EW1-RL17649995625EW1QGOn 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.

Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 07649995625046
Basic UDI-DI: 7649995625EW1QG
Reference / catalog number: EW1-RS1
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y060680UPPER LIMB ORTHOSES - ACCESSORIES

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
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Software identification