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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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PRIMUSmed - Erektionsring / erection… — 4 UDI-DI variants, MDR

MD Atlas
tic Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

PRIMUSmed - Erektionsring / erection ring

426021766-TA-RingeTN

4 UDI-DI variants

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

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

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426021766-TA-RingeTN
Device name: PRIMUSmed - Erektionsring / erection ring
Device model: PRIMUSmed
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: tic Medizintechnik GmbH
SRN: DE-MF-000033923
Country: Germany
Email: info@ticmed.de
Phone: +49236920850

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KGKS0FPK71M7XZCFJE05RDGQ

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

ti109504260217660756
ti109204260217660725
ti109404260217660749
ti109304260217660732