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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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Venner Medical (Deutschland) GmbH — Manufacturer in Germany

EUDAMED update: Jan 29, 2026

VM

Venner Medical (Deutschland) GmbH

Germany

All roles followed

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Sources: EUDAMED

Legal information of VMD

Legal name: Venner Medical (Deutschland) GmbH
EU VAT number: DE114182455
EORI: DE2693348
Trade register: HRB 10213 KI
SRN (displayed role): DE-MF-000005934
EUDAMED status: Active· registered in 2021
Registered office: Gut Uhlenhorst, 4 24229 Dänischenhagen, Germany

Contact details for VMD

Phone: +49(0)434991540
Email: info@vennermedical.de
Website: www.vennermedical.de
Address: 4, GUT UHLENHORST 24229 DÄNISCHENHAGEN GERMANY

Data export

Export the 27 devices of VMD

Get the catalogue in Excel or CSV format — trade name, product reference, UDI and EMDN codes, legislation, quantity, last update, and more. The exact row count and price are confirmed before you pay.

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SRNDE-MF-000005934

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Medical device companies in Germany

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Competent authority for VMD

DE/CA01 – Landesamt für Arbeitsschutz, Soziales und Gesundheit Schleswig-Holstein – Abteilung 3 Gesundheits- und Verbraucherschutz
GermanyContact the authority →

Certificates of VMD

27Total Devices

26Basic UDI-DIs

1Certificates1 valid · 0 expiring < 12 months

4CountriesEU/EEA placements

Market presence of VMD

Devices placed in 4 countries

Germany27
Austria21
Italy15
Romania15

Risk categories of VMD

Related documents of VMD

Quality management system

Certificate G10 067727 0011Rev. Rev. 00

Issued

Manufacturer

Venner Medical (Deutschland) GmbH

Notified body

TÜV SÜD Product Service GmbH

0123

Version

1

Valid from

7/18/2024

Valid until

7/17/2029

Executives & regulatory representatives of VMD

4 contacts identified

LEAÑO Gloria
PRRC
View profile →
ROBERTSON Jarrad
PRRC
View profile →
LEAÑO Gloria
As the primary PRRC, she fulfils the responsibilities defined in Article 15(3) of Regulation (EU) 2017/745, including oversight of device conformity, technical documentation, post-market surveillance, and vigilance obligations.
Hidden
ROBERTSON Jarrad
As the deputy PRRC, he acts only in the absence or unavailability of the primary PRRC and assumes full PRRC responsibilities during such periods.
Hidden

Cartography of VMD

ManufacturerImporterNotified bodiesPeople

VMD — DE-IM-000014678
VMD — DE-MF-000005934
TÜV SÜD Product Service GmbH — 1 certificate — VMD
LEAÑO Gloria — VMD
ROBERTSON Jarrad — VMD

Catalog of VMD

27 devices · 29 families

Filter

PEGA® BAG 50ml1 version
PEGA® BAG 100 ml1 version
PEGA® BAG 150 ml1 version
PEGA® BAG 300 ml1 version
PEGA® COMBI LINE S0 versions
PEGA® COMBI LINE E1 version
PEGA® COMBI LINE E with NRFit® connector1 version
PEGA® COMBI LINE Y1 version
PEGA® TUBE0 versions
PEGA® SPIKE0 versions
PEGA® SET 50 ml1 version
PEGA® SET 100 ml1 version
PEGA® SET 150 ml1 version
PEGA® SET 300 ml1 version
PEGA® SET curled 300 ml1 version
PEGA® SET curled 150 ml1 version
PEGA® SET curled 100 ml1 version
PEGA® SET curled 50 ml1 version
PEGA PCA Infusionspumpe1 version
PEGA plus Infsusionspumpe1 version
PEGA® COMBI LINE1 version
PEGA® SET1 version
PEGA® BAG1 version
PEGA® SPIKE1 version
PEGA® TUBE1 version

29 families

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Browse all 27 products