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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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SALSA HhaI — 1 UDI-DI variant, IVDR (MRC Holland B.V.)

MD Atlas
MRC Holland B.V.

Data from EUDAMED, last updated May 31, 2026

SALSA HhaI

872021148HhaIGP

1 UDI-DI variant

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: MRC Holland B.V.

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 872021148HhaIGP
Device name: SALSA HhaI
Device model: SMR50
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Feb 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: MRC Holland B.V.
SRN: NL-MF-000000437
Country: Netherlands
Email: qa-ra@mrcholland.com
Phone: +31 88 8657200

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KJ59DRZ4CAT38BKPWNCYBGEH

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

SMR5008720211482618