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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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Crossit — 3 UDI-DI variants, MDR (Careva System AB)

MD Atlas
Careva System AB

Data from EUDAMED, last updated May 30, 2026

Crossit

7350037450028W

3 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: 7350037450028W
Device name: —
Device model: Crossit
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

3 UDI-DI variants

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Applied filters

basicUdiUlid01JAAKXK0E43480DHX5RYCSB2S

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

Crossit07350037450303
Crossit 2.007350037450327
Crossit seat pad07350037450310