Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Primedistom — 497 UDI-DI variants, MDR

MD Atlas
Primed Halberstadt Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

Primedistom

42502032PRI06452

497 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Primed Halberstadt Medizintechnik GmbH

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42502032PRI06452
Device name: Primedistom
Device model: Trachealkanüle
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Apr 30, 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

497 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KQERZ49XRG4WC5G33HNMMRYC

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

201373 u04250203240925
20137304250203221672
20034304250203223683
201313 u04250203239493
200343 u04250203237161
20131304250203223751
20030304250203223515
20155604250203240628
20130304250203223416
201303 u04250203239257
201343 u04250203255516
201586 u04250203254823
200323 u04250203236881
20156604250203254441
20157604250203254564
201324 u04250203255325
20158604250203254809
201566 u04250203254465
20132404250203223843
201576 u04250203254588
20032304250203223607
200304 u04250203236645
20134404250203224000
20155704250203240635
201557 u04250203241922

5 6 7 8 9