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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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DELFIA Enhancement Solution — 3 UDI-DI variants, IVDR (Wallac Oy)

MD Atlas
Wallac Oy

Data from EUDAMED, last updated May 23, 2026

DELFIA Enhancement Solution

6438147D_ES6X

3 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Wallac Oy

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 6438147D_ES6X
Device name: DELFIA Enhancement Solution
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jul 1, 2022

Manufacturer & authorised representative

Manufacturer

Name: Wallac Oy
SRN: FI-MF-000022620
Country: Finland
Email: regulatoryaffairs.turku@revvity.com
Phone: +3582 2678111

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01G6T3XJN13WK5WAK0VGHW0R01

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

DELFIA Enhancement Solution06438147009725
DELFIA Enhancement Solution06438147005253
DELFIA Enhancement Solution06438147005260