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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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Pri-Pumpdrainagen — 8 UDI-DI variants, MDR

MD Atlas
Primed Halberstadt Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

Pri-Pumpdrainagen

42502032PRI0434S

8 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: Primed Halberstadt Medizintechnik GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42502032PRI0434S
Device name: —
Device model: Pri-Pumpdrainagen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 3, 2026

Manufacturer & authorised representative

Manufacturer

Name: Primed Halberstadt Medizintechnik GmbH
SRN: DE-MF-000004967
Country: Germany
Email: primed@primed-halberstadt.de
Phone: +4939416686

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01KGJ83A373N5EGEKJ7XPZ12ZB

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

2206904250203201889
2206004250203201797
2206104250203201803
2206204250203201810
2206304250203201827
2206404250203201834
2206504250203201841
2206604250203201858