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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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Rebel RA — 12 UDI-DI variants, MDR (Human Care HC AB)

MD Atlas
Human Care HC AB

Data from EUDAMED, last updated May 30, 2026

Rebel RA

7331599RH002231123421SN

12 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: Human Care HC AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7331599RH002231123421SN
Device name: Rebel RA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: Human Care HC AB
SRN: SE-MF-000002090
Country: Sweden
Email: info.se@humancaregroup.com
Phone: +46 8 510 132 00

Variants by status

UDI-DI variants

12 UDI-DI variants

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Applied filters

basicUdiUlid01KS7DEZ0RK96EGX53C17BF2QD

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

Rebel RA 6707331599223215
Rebel RA 67 Low07331599223116
Rebel RA 67 Low with seat07331599223550
Rebel RA 67 with seat07331599644898
Rebel RA 7207331599224212
Rebel RA 72 Low07331599224113
Rebel RA 72 Low with seat07331599644904
Rebel RA 72 with seat07331599644911
Rebel TW 6707331599233214
Rebel TW 67 Low07331599233115
Rebel TW 7207331599234211
Rebel TW 72 Low07331599234112