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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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SOFTKIT 2.0 BEIGE — 10 UDI-DI variants, MDR (Camp Scandinavia AB)

MD Atlas
Camp Scandinavia AB

Data from EUDAMED, last updated May 31, 2026

SOFTKIT 2.0 BEIGE

733094528749E2

10 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: Camp Scandinavia AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 733094528749E2
Device name: SOFTKIT 2.0 BEIGE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: Camp Scandinavia AB
SRN: SE-MF-000021395
Country: Sweden
Email: info@camp.se
Phone: +4642252700

Variants by status

UDI-DI variants

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JS19AQ1B67WM2WTFVVYV4XWS

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

SOFTKIT 2.0 BEIGE07330945735822
SOFTKIT 2.0 BEIGE07330945692217
SOFTKIT 2.0 BEIGE07330945692231
SOFTKIT 2.0 BEIGE07330945735839
SOFTKIT 2.0 BEIGE07330945692255
SOFTKIT 2.0 BEIGE07330945735846
SOFTKIT 2.0 BEIGE07330945692248
SOFTKIT 2.0 BEIGE07330945692224
SOFTKIT 2.0 BEIGE07330945735808
SOFTKIT 2.0 BEIGE07330945735815