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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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Silicone Foot Orthotic Devices… — 9 UDI-DI variants, MDR (Pletra Ltd.)

MD Atlas
Pletra Ltd.

Data from EUDAMED, last updated May 30, 2026

Silicone Foot Orthotic Devices (Footcare)

477904381FOOTCAREDV

9 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: Pletra Ltd.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 477904381FOOTCAREDV
Device name: —
Device model: Silicone Foot Orthotic Devices (Footcare)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: Pletra Ltd.
SRN: LT-MF-000004741
Country: Lithuania
Email: info@pletra.lt
Phone: +37068635757

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01KS7DMSY6BAPGNRHFN80924YH

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

Heel Pad Maxi04779043810346
Heel Pad Midi04779043810339
Heel Pad 36-3804779043811947
Heel Pad 39-4104779043811954
TARPUPIRSTIS-PLATUS04779043810308
Heel Pad 42-4404779043811961
TARPUPIRSTIS-SIAURAS04779043810292
Toe Spacer Flat04779043810315
Heel pad Mini04779043810322