Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Pain Patch — 7 UDI-DI variants, MDR (Cannordic A/S )

MD Atlas
Cannordic A/S

Data from EUDAMED, last updated May 30, 2026

Pain Patch

574400013MDPAIP21FT

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: Cannordic A/S

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Clinical investigations

Investigation number: 250103
Registered: No
Countries: India

Identity & classification

Basic UDI-DI: 574400013MDPAIP21FT
Device name: Pain Patch
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 9, 2024

Manufacturer & authorised representative

Manufacturer

Name: Cannordic A/S
SRN: DK-MF-000003852
Country: Denmark
Email: info@cannordic.com
Phone: +45 70 70 73 37

Variants by status

UDI-DI variants

7 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01HRRXV3SB09Z18650D3S6TWYG

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

PL-CSPP10030708594060120966
PL-CSPP10030105744000130491
87652A-IT08058363620986
PL-CSPP10030309120050883390
87652A05744000130590
PL-CSPP10030404260471893204
PL-CSPP10030505744000130736