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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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Patient Spirometry Tubes — 3 UDI-DI variants, MDR

MD Atlas
GE Healthcare Finland Oy

Data from EUDAMED, last updated May 23, 2026

Patient Spirometry Tubes

08406821BUG004797T

3 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: GE Healthcare Finland Oy

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 08406821BUG004797T
Device name: Patient Spirometry Tubes
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 3, 2025

Manufacturer & authorised representative

Manufacturer

Name: GE Healthcare Finland Oy
SRN: FI-MF-000001176
Country: Finland
Email: eudamed@gehealthcare.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01JZ7JBRE3ZVFYBAFPTPDE26WQ

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

89003100840682103701
891191-HEL00840682103619
88410100840682103626