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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

PRO13 — Class I MDD by VIXIMED AB

MD Atlas
VIXIMED AB

EUDAMED last updated this device on Apr 16, 2025

PRO13

B-VIEWMED_Encoder59

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: VIXIMED AB
UDI-DI code: D-VIEWMED_Encoder59
Reference / catalog number: PRO13

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View device family (Basic UDI)

Manufacturer information

Organization name: VIXIMED AB
SRN: SE-MF-000046510
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Sweden; available across 1 country total.

Placed on the market in Sweden; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: D-VIEWMED_Encoder59
Basic UDI-DI: B-VIEWMED_Encoder59
Reference / catalog number: PRO13
Issuing entity: EUDAMED

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: The intended use for the Viewmed Encoder is to distribute video and audio in real time to be used for consultation, documentation and education.
Additional information URL: https://viximed.se/contact
Clinical sizes: 3.5 MU10
14 MU10
13.5 MU10

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

D-VIEWMED_Encoder59

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Z119099VARIOUS BIOIMAGING AND RADIOTHERAPY INSTRUMENTS - 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

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Related devices

PRO04B-Viewmed-Single6NOn 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.