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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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Toe Spreader - Bunion Protector — 4 UDI-DI variants, MDR

MD Atlas
Bevaplast B.V.

Data from EUDAMED, last updated May 30, 2026

Toe Spreader - Bunion Protector

8712175_TD_13_TOEBUDB

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: Bevaplast B.V.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8712175_TD_13_TOEBUDB
Device name: Toe Spreader - Bunion Protector
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 25, 2024

Manufacturer & authorised representative

Manufacturer

Name: Bevaplast B.V.
SRN: NL-MF-000004386
Country: Netherlands
Email: sales@bevaplast.nl
Phone: +31 88 2382700

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HWA4ZKVZYCGY3D07WKV1SZCM

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

786308712175936528
792108712175937006
753604047196053263
795708712175937174