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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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Spirare Client — 2 UDI-DI variants, MDR (Diagnostica AS)

MD Atlas
Diagnostica AS

Data from EUDAMED, last updated May 30, 2026

Spirare Client

709003245SPDSWAY

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Diagnostica AS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 709003245SPDSWAY
Device name: Spirare Client
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 26, 2025

Manufacturer & authorised representative

Manufacturer

Name: Diagnostica AS
SRN: NO-MF-000041375
Country: Norway
Email: post@spirare.com
Phone: +4722924000

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JQ9Y4TH07HMD575WD30FB73Y

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

Spirare PC SPDSW007090032450013
Spirare Web SPDWB007090032450020