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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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Prismaflex HF20 set — 1 UDI-DI variant, MDR (Vantive Health GmbH)

MD Atlas
Vantive Health GmbH

Data from EUDAMED, last updated May 31, 2026

Prismaflex HF20 set

7332414VA00002733

1 UDI-DI variant

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

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

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7332414VA00002733
Device name: Prismaflex HF20 set
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: Vantive Health GmbH
SRN: CH-MF-000038981
Country: Switzerland
Email: fabrizio.pasqua@vantive.com
Phone: +41 7974 68 216

Authorised representative

Name: Vantive S.r.l.
SRN: IT-AR-000041309
Country: Italy

Variants by status

UDI-DI variants

1 UDI-DI variant

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basicUdiUlid01KS6XAF11D1JFVD6CAVAF30QW

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

Prismaflex HF20 set07332414201302