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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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Formalin 10 %, phosphate buffered pH… — 8 UDI-DI variants, IVDR

MD Atlas
Reagena Oy

Data from EUDAMED, last updated May 23, 2026

Formalin 10 %, phosphate buffered pH 7,2 incl. 4 % formaldehyde

643007445102256A2

8 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: Reagena Oy

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 643007445102256A2
Device name: Formalin 10 %, phosphate buffered pH 7,2 incl. 4 % formaldehyde
Device model: 102256
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Feb 4, 2022

Manufacturer & authorised representative

Manufacturer

Name: Reagena Oy
SRN: FI-MF-000002804
Country: Finland
Email: info@reagena.com
Phone: +358 10 5045 200

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01FTTG0NDKEZWJWZDGGZ21P56T

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

18225606430074450861
11225606430074450854
1U225606430074450847
102256T06430074450830
1E225606430074450878
19225606430074450885
102256C706430074450816
102256C806430074450809