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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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Plasma Care — 4 UDI-DI variants, MDR (terraplasma medical GmbH)

MD Atlas
terraplasma medical GmbH

Data from EUDAMED, last updated May 23, 2026

Plasma Care

426064454PCR6

4 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: terraplasma medical GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426064454PCR6
Device name: Plasma Care
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 4, 2022

Manufacturer & authorised representative

Manufacturer

Name: terraplasma medical GmbH
SRN: DE-MF-000011250
Country: Germany
Email: info@terraplasma-medical.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01FZAJ0NNXPWN2R3M94Y90XMYK

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

PC100011 04260644540652
PC100012 04260644540669
PC10000104260644540102
plasma care spacer04260644540126