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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

MID-Comp — Class I MDR by Medical Innovation…

MD Atlas
Medical Innovation Design MID AB

EUDAMED last updated this device on Apr 30, 2026

MID-Comp

73501328MC06GX

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Medical Innovation Design MID AB
UDI-DI code: 07350132811740
Reference / catalog number: 21

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Manufacturer information

Organization name: Medical Innovation Design MID AB
SRN: SE-MF-000053189
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.

Country	On market since	Until
SwedenPrimary placement	Jan 1, 2026	Still on market

Device identification

Trade name: MID-Comp
UDI-DI code: 07350132811740
Basic UDI-DI: 73501328MC06GX
Reference / catalog number: 21
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: Easy handling – Smooth roller blind effect on the compression strap, without the need for a crank device. Elegant and functional design – Modern aesthetics combined with a surface that is easy to clean. Highest quality – All components are replaceable for long durability and reduced wear. Complete solution – Wall stand included for easy assembly and stable use.
Additional information URL: https://www.mid.nu/produkter/mid-comp-siemens-ysio-artnr-mc06-0308
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)07350132811740

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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.

Z11030580RADIOLOGY INSTRUMENTS - HARDWARE 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

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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.