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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-PP and E-PT — 2 UDI-DI variants, MDR (GE Healthcare Finland Oy)

MD Atlas
GE Healthcare Finland Oy

Data from EUDAMED, last updated May 23, 2026

E-PP and E-PT

8406821BUG00436HM

2 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: 8406821BUG00436HM
Device name: E-PP and E-PT
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Aug 22, 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

2 UDI-DI variants

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Applied filters

basicUdiUlid01J5X01895J1WPQJWV43TNPABF

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-PT-0000840682104128
E-PP-0000840682104159