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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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Extracorporeal tubing set — 8 UDI-DI variants, MDR (GVS S.p.A.)

MD Atlas
GVS S.p.A.

Data from EUDAMED, last updated May 31, 2026

Extracorporeal tubing set

805387980HL006C6

8 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: 805387980HL006C6
Device name: Extracorporeal tubing set
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 28, 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

8 UDI-DI variants

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Applied filters

basicUdiUlid01KSQNW1G17A719XPPAM4BNGXX

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

150000440608053879801133
150009440608053879801140
150099440608053879801171
150090440608053879801188
150019440608053879801164
150001440608053879801157
150901440608053879801195
150919440608053879801201