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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

14010040 — Class I MDR by Par Scientific Denmark…

MD Atlas
Par Scientific Denmark ApS

EUDAMED last updated this device on Mar 18, 2026

14010040

5745000245VacFixN5

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Par Scientific Denmark ApS
UDI-DI code: 05745000245345
Reference / catalog number: 14010040

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Manufacturer information

Organization name: Par Scientific Denmark ApS
SRN: DK-MF-000011892
Manufacturer status: Active

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2451001105745000245VacFixN5On the market 145100605745000245VacFixN5On the market 2101001005745000245VacFixN5On the market 40294,55745000245VacFixN5On the market 20080655745000245VacFixN5On the market

Market distribution

Primary placement in Denmark; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 05745000245345
Basic UDI-DI: 5745000245VacFixN5
Reference / catalog number: 14010040
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: Stereotactic body frame 140 x 100 cm, 40 liter
Additional information URL: https://www.parscientific.com/VacuumCushions.html
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V080302PATIENT POSITIONING MEDICAL CUSHIONS

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.