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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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MANNITOL NITRATE MOTILITY MEDIUM — 4 UDI-DI variants, IVDR

MD Atlas
Laboratorios Conda S.A.

Data from EUDAMED, last updated May 23, 2026

MANNITOL NITRATE MOTILITY MEDIUM

843529511509FP

4 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: Laboratorios Conda S.A.

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 843529511509FP
Device name: MANNITOL NITRATE MOTILITY MEDIUM
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jul 14, 2022

Manufacturer & authorised representative

Manufacturer

Name: Laboratorios Conda S.A.
SRN: ES-MF-000025575
Country: Spain
Email: alvaro.prieto@condalab.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G7XS4PJS6W7P3EF2CX90308Z

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

MANNITOL NITRATE MOTILITY MEDIUM08435295150659
MANNITOL NITRATE MOTILITY MEDIUM08435295128603
MANNITOL NITRATE MOTILITY MEDIUM08435295150666
MANNITOL NITRATE MOTILITY MEDIUM08435295150673