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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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Protac KneedMe — 6 UDI-DI variants, MDR (Protac A/S)

MD Atlas
Protac A/S

Data from EUDAMED, last updated May 23, 2026

Protac KneedMe

571488270075FV

6 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: Protac A/S

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 571488270075FV
Device name: Protac KneedMe
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 11, 2023

Manufacturer & authorised representative

Manufacturer

Name: Protac A/S
SRN: DK-MF-000000963
Country: Denmark
Email: protac@protac.dk
Phone: +45 86 19 41 03

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01H7FT3M3AY98V67QHY0BV6P50

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

700-751-3820-4005714882012970
700-751-3820-4105714882012994
700-751-3820-3005714882012956
700-755-U-3820-3005714882013038
700-755-U-3820-8005714882013076
Protac KneedMe To Go05714882013052