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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

InVision — Class I MDR by Medicinsk Bildteknik…

MD Atlas
Medicinsk Bildteknik Sverige AB

EUDAMED last updated this device on Nov 12, 2025

InVision

735016662InVisionEK

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Medicinsk Bildteknik Sverige AB
UDI-DI code: 17350166620018
Reference / catalog number: InV004

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View device family (Basic UDI)

Manufacturer information

Organization name: Medicinsk Bildteknik Sverige AB
SRN: SE-MF-000016899
Manufacturer status: Active

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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

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: InVision
UDI-DI code: 17350166620018
Basic UDI-DI: 735016662InVisionEK
Reference / catalog number: InV004
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: InVision is an integrated, modular software solution to view, record, store and distribute audio, video and image sources in (or between) hospitals. The product is intended for healthcare professionals.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)17350166620018

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

Z119007IMAGE ACQUISITION MODULES

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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