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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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Infusion Devices Class IIa — 68 UDI-DI variants, MDR (GVS S.p.A.)

MD Atlas
GVS S.p.A.

Data from EUDAMED, last updated Jun 2, 2026

Infusion Devices Class IIa

805387980SETINF2A0000003T

68 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: GVS S.p.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805387980SETINF2A0000003T
Device name: Infusion Devices Class IIa
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jun 1, 2026

Manufacturer & authorised representative

Manufacturer

Name: GVS S.p.A.
SRN: IT-MF-000028147
Country: Italy
Email: info@gvs.com
Phone: +39 0516176311

Variants by status

UDI-DI variants

68 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KT20E54HTZNSBXS4KG6T21D2

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

No registered UDI-DI variants for this device family.