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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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VM32SF.0 — 4 UDI-DI variants, MDR (Rein medical GmbH)

MD Atlas
Rein medical GmbH

Data from EUDAMED, last updated May 23, 2026

VM32SF.0

406163100000VM32SF0LM

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: Rein medical GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 406163100000VM32SF0LM
Device name: VM32SF.0
Device model: Video-Monitor
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 8, 2022

Manufacturer & authorised representative

Manufacturer

Name: Rein medical GmbH
SRN: DE-MF-000018721
Country: Germany
Email: info@reinmedical.com
Phone: +49216169840

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01FZSKPGJFAHA4AZ3N1E6ZXF7B

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

C432DS-DM204061631323230
C432DS-DM104061631323223
CLINIO 432DS04061631323209
CLINIO 432DS3-AIMS0104061631323216