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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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BevistoSept plus — 8 UDI-DI variants, MDR (BEVISTON GmbH)

MD Atlas
BEVISTON GmbH

Data from EUDAMED, last updated May 23, 2026

BevistoSept plus

42519522BevistoSeptplus2C

8 UDI-DI variants

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

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

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42519522BevistoSeptplus2C
Device name: BevistoSept plus
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 13, 2023

Manufacturer & authorised representative

Manufacturer

Name: BEVISTON GmbH
SRN: DE-MF-000015203
Country: Germany
Email: a.wettwer@beviston.com
Phone: 047411819830

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01GXWPW2FEX315A5KKF15VQJX7

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

207304251952220732
210004251952221005
207004251952220701
207104251952220718
209004251952220909
209104251952220916
209204251952220923
209304251952220930