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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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IMPACT sterile single use syringe — 2 UDI-DI variants, MDR

MD Atlas
Plasmaconcept AG

Data from EUDAMED, last updated May 23, 2026

IMPACT sterile single use syringe

426053139IMP211000E6

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Plasmaconcept AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426053139IMP211000E6
Device name: IMPACT sterile single use syringe
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jul 3, 2025

Manufacturer & authorised representative

Manufacturer

Name: Plasmaconcept AG
SRN: DE-MF-000005281
Country: Germany
Email: info@plasmaconcept.de
Phone: +49 (0)221 845625-0

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JZ7Y8K2VJK1S8CB0HV0V30PF

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

21120004260531390124
IMPACT sterile single-use syringe04260531390155