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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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Futura — 15 UDI-DI variants, MDR (Novista of Sweden AB)

MD Atlas
Novista of Sweden AB

Data from EUDAMED, last updated May 31, 2026

Futura

735008131F6X

15 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: Novista of Sweden AB

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Device characteristics

Active device

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 735008131F6X
Device name: Futura
Device model: Weight Duvet Futura
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: Novista of Sweden AB
SRN: SE-MF-000045071
Country: Sweden
Email: info@novista.se

Variants by status

UDI-DI variants

15 UDI-DI variants

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Applied filters

basicUdiUlid01KFARFE5T36ENM5Q5FSRQTW1S

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

Futura 10 kg07350081310837
Futura 12 kg07350081310844
Futura 14 kg07350081310851
Futura 140 10 kg07350081311438
Futura 140 12 kg07350081311445
Futura 140 14 kg07350081311452
Futura 140 4 kg07350081311407
Futura 140 6 kg07350081311414
Futura 140 8 kg07350081311421
Futura 2.3 kg07350081310868
Futura 3.7 kg07350081310875
Futura 4 kg07350081310806
Futura 5.0 kg07350081310882
Futura 6 kg07350081310813
Futura 8 kg07350081310820