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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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Diluent pH-7 — 6 UDI-DI variants, IVDR (Labex Reagens AB)

MD Atlas
Labex Reagens AB

Data from EUDAMED, last updated May 31, 2026

Diluent pH-7

73501450010021002SX

6 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: Labex Reagens AB

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 73501450010021002SX
Device name: Diluent pH-7
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 6, 2026

Manufacturer & authorised representative

Manufacturer

Name: Labex Reagens AB
SRN: SE-MF-000048594
Country: Sweden
Email: labex@labex.com
Phone: +4642324000

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQYWS69E4WDP5WN567GZ0DF3

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

TV00307350145000339
TV00207350145000322
TV003-1207350145000346
TV00107350145000315
TV001CT07350145000483
TV002CT07350145000490