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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

MD Atlas
Haemotronic S. p. A

Data from EUDAMED, last updated May 30, 2026

Extracorporeal tubing set

8033718HL006NL

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: Haemotronic S. p. A

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8033718HL006NL
Device name: Extracorporeal tubing set
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jun 3, 2025

Manufacturer & authorised representative

Manufacturer

Name: Haemotronic S. p. A
SRN: IT-MF-000029734
Country: Italy
Email: regulatory.ht.eu@gvs.com
Phone: +39 0535 619611

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01JW6FXR32K9FX3PB02YNHGFNK

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

150009440608033718001344
150000440608033718001337
150099440608033718001375
150090440608033718001382
150001440608033718001351
150019440608033718001368
150919440608033718001405
150901440608033718001399