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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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InviSorb® Spin Blood Mini Kit — 2 UDI-DI variants, IVDR

MD Atlas
ALS Life Sciences Portugal, S.A.

Data from EUDAMED, last updated May 31, 2026

InviSorb® Spin Blood Mini Kit

5600236235AA003E5

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: ALS Life Sciences Portugal, S.A.

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 5600236235AA003E5
Device name: InviSorb® Spin Blood Mini Kit
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: ALS Life Sciences Portugal, S.A.
SRN: PT-MF-000034751
Country: Portugal
Email: geral@alsglobal.com
Phone: (+351) 232 817 817

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KSQNK180GW8VXFBZ6DV4MPWT

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

1031100300 05600236235204
103110020005600236235198