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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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HYDRASYS 5 von WILLEBRAND MULTIMERS… — 2 UDI-DI variants, IVDR (sebia)

MD Atlas
sebia

Data from EUDAMED, last updated May 19, 2026

HYDRASYS 5 von WILLEBRAND MULTIMERS ACCESSORIES

3607361651BUD7

2 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: sebia

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 3607361651BUD7
Device name: HYDRASYS 5 von WILLEBRAND MULTIMERS ACCESSORIES
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jul 19, 2022

Manufacturer & authorised representative

Manufacturer

Name: sebia
SRN: FR-MF-000003520
Country: France
Email: acollin@sebia.com
Phone: +33 1 69 89 83 31

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01G7VBEKK9BD8752N8QSVKVPYH

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

HYDRASYS 11 von WILLEBRAND MULTIMERS ACCESSORIES03607360016534
HYDRASYS 5 von WILLEBRAND MULTIMERS ACCESSORIES03607360016510