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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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SigmaVision® Advanced — 2 UDI-DI variants, MDR

MD Atlas
Dr. Sennewald Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

SigmaVision® Advanced

PP12868SIGMAVISION33

2 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: Dr. Sennewald Medizintechnik GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: PP12868SIGMAVISION33
Device name: SigmaVision® Advanced
Issuing agency: IFA
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Special device type: refdata.special-mdr-device-type.software
Version date: May 16, 2024

Manufacturer & authorised representative

Manufacturer

Name: Dr. Sennewald Medizintechnik GmbH
SRN: DE-MF-000007093
Country: Germany
Email: maria.kerstens@sennewald.de
Phone: +49 89 54 21 43 10

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HY0GFGT988WF5Q8W8ZN376EH

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

010-260-2.0.11312868SIGMAVISION-2.0.X063
010-260-DONGLE1312868SIGMAVISIONDONGLE088