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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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Forceps — 2 UDI-DI variants, MDR (TITAMED)

MD Atlas
TITAMED

Data from EUDAMED, last updated May 23, 2026

Forceps

54040243BASIC0135C

2 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: TITAMED

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 54040243BASIC0135C
Device name: Forceps
Device model: Forceps
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 22, 2025

Manufacturer & authorised representative

Manufacturer

Name: TITAMED
SRN: BE-MF-000000110
Country: Belgium
Email: info@titamed.be
Phone: +32 (0)3 289 51 56

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01K38DYZ2WYHA14WWERMBHQXEH

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

Plate holding forceps, angled05404024308459
Plate holding forceps, straight05404024308442