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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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NuvoAir Home — 1 UDI-DI variant, MDD (NuvoAir AB)

MD Atlas
NuvoAir AB

Data from EUDAMED, last updated May 30, 2026

NuvoAir Home

B-07350002630051

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class I

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Manufacturer: NuvoAir AB

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Device characteristics

Active deviceMeasuring function

Legacy certificates

Certificate number: FI15/07005
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: SGS FIMKO OY (598 )
Validity: Dec 31, 2028

Identity & classification

Basic UDI-DI: B-07350002630051
Device name: NuvoAir Home
Device model: NVH-01
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Version date: May 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: NuvoAir AB
SRN: SE-MF-000005645
Country: Sweden
Email: mircea.campian@nuvoair.com
Phone: +31 614591185

Variants by status

UDI-DI variants

1 UDI-DI variant

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basicUdiUlid01KRG84S6RTSA00M0C6RSG4B5G

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

NuvoAir Home07350002630051