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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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HITSD Red — 17 UDI-DI variants, MDR (C-RAD Positioning AB)

MD Atlas
C-RAD Positioning AB

Data from EUDAMED, last updated May 30, 2026

HITSD Red

735000528HITED

17 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: C-RAD Positioning AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 735000528HITED
Device name: HITSD Red
Device model: HITSD Red
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 15, 2022

Manufacturer & authorised representative

Manufacturer

Name: C-RAD Positioning AB
SRN: SE-MF-000022326
Country: Sweden
Email: info@c-rad.com
Phone: +46 18 410 8288

Variants by status

UDI-DI variants

17 UDI-DI variants

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Applied filters

basicUdiUlid01G2T8R26X5MGQR95WVPX24PZG

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

SP007-000117350005280441
SP007-002117350005280465
SP007-001117350005280458
SP006-000217350005280472
SP006-002217350005280496
SP006-001217350005280489
SP006-000317350005280502
SP006-002317350005280526
SP006-001317350005280519
SP006-000417350005280533
SP006-000117350005280410
SP006-002117350005280434
SP006-001117350005280427
SP005-000217350005280397
SP005-000617350005280403
SP005-000517350005280649
SP005-000117350005280380