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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

Pollux Carrier StretchTrolley 1080 — Class I MDR

MD Atlas
MA-GO Scandinavia AB

EUDAMED last updated this device on Apr 13, 2026

Pollux Carrier StretchTrolley 1080

735013213PolluxCarrier99

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MA-GO Scandinavia AB
UDI-DI code: 17350132130022
Reference / catalog number: 310230100

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View device family (Basic UDI)

Manufacturer information

Organization name: MA-GO Scandinavia AB
SRN: SE-MF-000004856
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	May 20, 2022	Still on market

Device identification

Trade name: Pollux Carrier StretchTrolley 1080
UDI-DI code: 17350132130022
Basic UDI-DI: 735013213PolluxCarrier99
Reference / catalog number: 310230100
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: Bårtransportvagn, helikopter och bår av typ Cirrus, lasthöjd 1080 mm. Används tillsammans med helikopterbår Aerolite Cirrus, Pensibår, Allfabår och transportkuvös Airborne. Bårtransportvagnen är anpassad för att passa helikoptertypen AW 169, med lasthöjd 1080 mm.
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)17350132130022

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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.

Y122799NON-MOTORIZED VEHICLES AND MEANS OF TRANSPORT - 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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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.