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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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VISMED® — 7 UDI-DI variants, MDR (TRB Chemedica AG)

MD Atlas
TRB Chemedica AG

Data from EUDAMED, last updated May 23, 2026

VISMED®

4028694VISMED3F

7 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: TRB Chemedica AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4028694VISMED3F
Device name: VISMED®
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Aug 7, 2025

Manufacturer & authorised representative

Manufacturer

Name: TRB Chemedica AG
SRN: DE-MF-000006919
Country: Germany
Email: info@trbchemedica.de
Phone: +49 (0)89 46 14 83 0

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01K21TBEXT9PSZQGMBGWPNSHBM

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

HYLOVIS®04028694001369
HYLOVIS®04028694001406
0402869400121504028694001215
0402869400013304028694000133
0402869400139004028694001390
0402869400137604028694001376
0402869400097304028694000973