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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

10253 — Class I MDR by Villa Manus Oy

MD Atlas
Villa Manus Oy

EUDAMED last updated this device on Nov 26, 2021

10253

642981065710253MX

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Villa Manus Oy
UDI-DI code: 06429810657114
Reference / catalog number: 10253

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Manufacturer information

Organization name: Villa Manus Oy
SRN: FI-MF-000007871
Manufacturer status: Active

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10222E642981065710222EK8On the market 10119E642981065710119EKHOn the market 10117E642981065710117EKBOn the market 10154E642981065710154EKNOn the market 10120E642981065710120EJTOn the market

Market distribution

Primary placement in Finland; available across 2 countries total.

Country	On market since	Until
FinlandPrimary placement		Still on market
Sweden		Still on market

Device identification

Trade name: not provided
UDI-DI code: 06429810657114
Basic UDI-DI: 642981065710253MX
Reference / catalog number: 10253
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: 20 x 30 cm

EMDN nomenclature code(s)

Y060699ORTHOSES, UPPER EXTREMITY - 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

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.