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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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PLANTILLA FASCITIS PLANTAR — 4 UDI-DI variants, MDR (Flexor S.A.)

MD Atlas
Flexor S.A.

Data from EUDAMED, last updated May 23, 2026

PLANTILLA FASCITIS PLANTAR

84355156fascitis1096BR

4 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.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84355156fascitis1096BR
Device name: PLANTILLA FASCITIS PLANTAR
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 12, 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

4 UDI-DI variants

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Applied filters

basicUdiUlid01KC90X26DC6E85KABC6KWVZQD

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

1096.500 EG08430469237778
1096.500 G08430469237761
1096.500 M08430469237754
1096.500 P08430469237747