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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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Vivid E95_Vivid E90_Vivid E80 — 4 UDI-DI variants, MDR

MD Atlas
GE Vingmed Ultrasound AS

Data from EUDAMED, last updated May 30, 2026

Vivid E95_Vivid E90_Vivid E80

8406821BUG00253HB

4 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: GE Vingmed Ultrasound AS

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 8406821BUG00253HB
Device name: —
Device model: Vivid E95_Vivid E90_Vivid E80
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 27, 2022

Manufacturer & authorised representative

Manufacturer

Name: GE Vingmed Ultrasound AS
SRN: NO-MF-000000553
Country: Norway
Email: eudamed@gehealthcare.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FSSBPKJCDQPA1C28G0PWXSZT

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

Vivid E80 v20600195278505347
Vivid E90 v20600195278505354
Vivid E95 v20600195278505330
Vivid E v203 v204 to v206 UPG00195278516343