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.

FLEXOR MEDICAL CARE FASCITIS PLANTAR — 6 UDI-DI variants, MDR

MD Atlas
Flexor S.A.

Data from EUDAMED, last updated May 23, 2026

FLEXOR MEDICAL CARE FASCITIS PLANTAR

84355156FM6260CL

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: Flexor S.A.

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

Identity & classification

Basic UDI-DI: 84355156FM6260CL
Device name: FLEXOR MEDICAL CARE FASCITIS PLANTAR
Device model: FLEXOR MEDICAL CARE FASCITIS PLANTAR
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 8, 2025

Manufacturer & authorised representative

Manufacturer

Name: Flexor S.A.
SRN: ES-MF-000042891
Country: Spain
Email: quality@flexor.es
Phone: +34 93 718 16 12

Variants by status

UDI-DI variants

6 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

basicUdiUlid01K4MGXVZKAVYX6S73G9AVP5HN

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

FM6 260 35/3608435515600292
FM6 260 37/3808435515600308
FM6 260 39/4008435515600315
FM6 260 41/4208435515600322
FM6 260 43/4408435515600339
FM6 260 45/4608435515600346