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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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9T — 2 UDI-DI variants, MDR (GE Vingmed Ultrasound AS)

MD Atlas
GE Vingmed Ultrasound AS

Data from EUDAMED, last updated May 30, 2026

9T

8406821BUG00006GQ

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: GE Vingmed Ultrasound AS

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8406821BUG00006GQ
Device name: 9T
Device model: 9T
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Aug 8, 2023

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

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H7AQR5AKFKVPX67BVDFJ6XRD

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

KN10012100840682115636
KN10012200840682115728