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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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KIDDIEFLOW — 7 UDI-DI variants, MDR (Camp Scandinavia AB)

MD Atlas
Camp Scandinavia AB

Data from EUDAMED, last updated May 30, 2026

KIDDIEFLOW

733094528890E4

7 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: 733094528890E4
Device name: KIDDIEFLOW
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 27, 2024

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

7 UDI-DI variants

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Applied filters

basicUdiUlid01HSZMZXZYS8GFQ3Y7Y9PAV7DJ

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

KIDDIEFLOW07330945823130
KIDDIEFLOW07330945823123
KIDDIEFLOW07330945823079
KIDDIEFLOW07330945823062
KIDDIEFLOW07330945823093
KIDDIEFLOW07330945823109
KIDDIEFLOW07330945823086