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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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Head Caps — 13 UDI-DI variants, MDR (Ultratex GmbH)

MD Atlas
Ultratex GmbH

Data from EUDAMED, last updated May 23, 2026

Head Caps

426073948101B4

13 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: Ultratex GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426073948101B4
Device name: Head Caps
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 16, 2022

Manufacturer & authorised representative

Manufacturer

Name: Ultratex GmbH
SRN: DE-MF-000005415
Country: Germany
Email: info@ultratex.com
Phone: +49 241 156094

Variants by status

UDI-DI variants

13 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GHZYK9XBSMQX8XKFPHADRZ04

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

101-0104260739480146
10104260739481013
101-0404260739481143
103-0104260739481334
103-0204260739481341
10304260739481310
102-0204260739481235
101-0204260739480139
101-03104260739480153
102-0304260739481242
102-0104260739480160
101-0304260739481136
10204260739481211