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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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Ankle Brace — 10 UDI-DI variants, MDR (Burman Enterprise)

MD Atlas
Burman Enterprise

Data from EUDAMED, last updated May 30, 2026

Ankle Brace

819504020717CR

10 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: Burman Enterprise

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 819504020717CR
Device name: Ankle Brace
Device model: B09LLMP3XL
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 28, 2025

Manufacturer & authorised representative

Manufacturer

Name: Burman Enterprise
SRN: SE-MF-000048669
Country: Sweden
Email: cazarah@sleevestars.com

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01K0V98A3EMYFAJY4BXQG3E5NC

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

B09NXNXVX800819504020786
B09LLPDTYV00819504020731
B09LV69LFJ00819504020755
B0C3LM8CH600819504020939
B0C3LLBGM200819504020908
Ankle Brace00639385745673
B09LLX9XNY00819504020724
B09LLQ78CD00819504020748
B09LLMP3XL00819504020717
B09LV4M57800819504020779