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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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ACTIVE X KNEE PATELLA — 5 UDI-DI variants, MDR (Camp Scandinavia AB)

MD Atlas
Camp Scandinavia AB

Data from EUDAMED, last updated May 30, 2026

ACTIVE X KNEE PATELLA

733094528055CS

5 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: 733094528055CS
Device name: ACTIVE X KNEE PATELLA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 19, 2023

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

5 UDI-DI variants

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Applied filters

basicUdiUlid01H5PN843M7NWX6151QTFD0757

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

ACTIVE X KNEE PATELLA07330945685554
ACTIVE X KNEE PATELLA07330945685530
ACTIVE X KNEE PATELLA07330945685547
ACTIVE X KNEE PATELLA07330945685523
ACTIVE X KNEE PATELLA07330945685561