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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

MW3-PS1 — Class IIa MDR by USMIMA, S.L.

MD Atlas
USMIMA, S.L.

EUDAMED last updated this device on Aug 26, 2025

MW3-PS1

8437016001MOWOOTII7E

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: USMIMA, S.L.
UDI-DI code: 08437016001158
Reference / catalog number: MW3-PS1

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Manufacturer information

Organization name: USMIMA, S.L.
SRN: ES-MF-000000232
Manufacturer status: Active

Related devices

MW2-D018437016001MOWOOTII7EOn the market MW2-B038437016001MOWOOTII7EOn the market MW2-B028437016001MOWOOTII7EOn the market MW2-B048437016001MOWOOTII7EOn the market MW2-B018437016001MOWOOTII7EOn 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 Spain; available across 2 countries total.

Country	On market since	Until
SpainPrimary placement	Aug 25, 2025	Still on market
Germany	Aug 25, 2025	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08437016001158
Basic UDI-DI: 8437016001MOWOOTII7E
Reference / catalog number: MW3-PS1
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: DC Power Adapter; For indoor use only. Receives 100-240 VAC, 50-60 Hz and supplies 12 VDC 2A to the desktop device.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

G99GASTROINTESTINAL DEVICES - 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
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Software identification