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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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Pollux Carrier StretchTrolley — 5 UDI-DI variants, MDR

MD Atlas
MA-GO Scandinavia AB

Data from EUDAMED, last updated May 31, 2026

Pollux Carrier StretchTrolley

735013213PolluxCarrier99

5 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: MA-GO Scandinavia AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 735013213PolluxCarrier99
Device name: —
Device model: Pollux Carrier StretchTrolley
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: MA-GO Scandinavia AB
SRN: SE-MF-000004856
Country: Sweden
Email: info@mago.se
Phone: +46 500484974

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KP2GRFS080ZCRW0ZVK7W4Q0H

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

Pollux Carrier IncubatorTrolley17350132130053
Pollux Carrier IncubatorTrolley AV17350132130060
Pollux Carrier StrechTrolley17350132130077
Pollux Carrier StretchTrolley 108017350132130022
Pollux Carrier StretchTrolley 99017350132130046