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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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Respiro Accessories — 10 UDI-DI variants, MDR (Bittium Biosignals Oy)

MD Atlas
Bittium Biosignals Oy

Data from EUDAMED, last updated May 23, 2026

Respiro Accessories

643003522RespiroAccLK

10 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: Bittium Biosignals Oy

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 643003522RespiroAccLK
Device name: Respiro Accessories
Device model: Respiro Accessories
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 3, 2025

Manufacturer & authorised representative

Manufacturer

Name: Bittium Biosignals Oy
SRN: FI-MF-000013983
Country: Finland
Email: bbs@bittium.com

Variants by status

UDI-DI variants

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K94FG60ZKASH16Z6H0XB804J

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

930540206430035221165
940477706430035221172
930540306430035221189
940477806430035221196
930557606430035221202
940478106430035221219
S000002035206430035221141
S000002036806430035221158
S000002034506430035221127
S000002036306430035221134