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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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Careva Systems — 37 UDI-DI variants, MDR (Careva System AB)

MD Atlas
Careva System AB

Data from EUDAMED, last updated May 30, 2026

Careva Systems

7350037450018U

37 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: Careva System AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7350037450018U
Device name: —
Device model: Careva Systems
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 16, 2024

Manufacturer & authorised representative

Manufacturer

Name: Careva System AB
SRN: SE-MF-000004861
Country: Sweden
Email: info@careva.se
Phone: +46 31 22 28 00

Variants by status

UDI-DI variants

37 UDI-DI variants

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Applied filters

basicUdiUlid01JAA9SRX8XRJXW89HHAGKXTMZ

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

Shoulder belt07350037450136
Shoulder belt L07350037450150
Shoulder belt M07350037450143
Shoulder KIT07350037450334
Shoulder KIT07350037450358
Shoulder KIT07350037450341
Spinal belt07350037450020
Spinal belt S07350037450013
Standard buckle m07350037450099
Standard buckle metallic07350037450075
Standard buckle p07350037450105
Standard buckle plastic07350037450082

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