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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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E-sCO, E-sCOV, E-sCOVX, E-sCAiO,… — 9 UDI-DI variants, MDR

MD Atlas
GE Healthcare Finland Oy

Data from EUDAMED, last updated May 23, 2026

E-sCO, E-sCOV, E-sCOVX, E-sCAiO, E-sCAiOV, E-sCAiOVX, E-sCAiOE, E-sCAiOVE, N-CAiO

08406821BUG004677L

9 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: GE Healthcare Finland Oy

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 08406821BUG004677L
Device name: E-sCO, E-sCOV, E-sCOVX, E-sCAiO, E-sCAiOV, E-sCAiOVX, E-sCAiOE, E-sCAiOVE, N-CAiO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jun 17, 2024

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

9 UDI-DI variants

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Applied filters

basicUdiUlid01J0JVHMDRD33K4KGDR18T9YY1

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

E-sCO-0000840682104173
E-sCAiOVE-0000840682104302
N-CAiO-0000840682104074
E-sCAiOV-0000840682104142
E-sCAiOE-0000840682104135
E-sCOV-0000840682104258
E-sCOVX-0000840682104289
E-sCAiO-0000840682104180
E-sCAiOVX-0000840682104067