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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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Liquid Acid Concentrate for… — 2 UDI-DI variants, MDR (Sterima)

MD Atlas
Sterima

Data from EUDAMED, last updated May 30, 2026

Liquid Acid Concentrate for bicarbonate based HD, HDF and HF

5412977AconcentratePK

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Sterima

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5412977AconcentratePK
Device name: Liquid Acid Concentrate for bicarbonate based HD, HDF and HF
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Sterima
SRN: BE-MF-000017855
Country: Belgium
Email: info@sterima.be
Phone: +32 56 36 13 11

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KSHPJFY1AC8WXDS45TT4X1MG

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

Solhemo05412977000986
3042500009805412977000252