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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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ViewPoint 6 — 2 UDI-DI variants, MDR (GE Healthcare GmbH)

MD Atlas
GE Healthcare GmbH

Data from EUDAMED, last updated May 23, 2026

ViewPoint 6

8406821BUG00018GX

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 Healthcare GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8406821BUG00018GX
Device name: ViewPoint 6
Device model: ViewPoint 6
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Jul 29, 2022

Manufacturer & authorised representative

Manufacturer

Name: GE Healthcare GmbH
SRN: DE-MF-000005087
Country: Germany
Email: eudamed@gehealthcare.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G938KRM4WV5K2EKHPQWDERF4

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

ViewPoint 600195278517340
594520900195278753472