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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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Elektrodenkontaktspray — 9 UDI-DI variants, MDR

MD Atlas
C+V Pharma Depot GmbH

Data from EUDAMED, last updated May 23, 2026

Elektrodenkontaktspray

PP05199EKS22

9 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: C+V Pharma Depot GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: PP05199EKS22
Device name: Elektrodenkontaktspray
Issuing agency: IFA
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 21, 2024

Manufacturer & authorised representative

Manufacturer

Name: C+V Pharma Depot GmbH
SRN: DE-MF-000022382
Country: Germany
Email: qm@cundv.de

Variants by status

UDI-DI variants

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JD7SP3NXPH8CFS8SFTX1HMJ1

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

11193953721900111939537219
11193954036600111939540366
11195491315600111954913156
A00001170112022487146
A00001237112022488836
11193801815000111938018150
11193801758400111938017584
11193953890900111939538909
11193801692100111938016921