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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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T-Tuben — 7 UDI-DI variants, MDR

MD Atlas
Primed Halberstadt Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

T-Tuben

42502032PRI05959

7 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: 42502032PRI05959
Device name: —
Device model: T-Tuben
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 26, 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

7 UDI-DI variants

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Applied filters

basicUdiUlid01KFWXYZXWKPNXK8V3XV4Y10PF

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

20064204250203221184
20064304250203221191
20064404250203221207
20064504250203221214
20064604250203221221
20064004250203221160
20064104250203221177