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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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Aparat korekcyjny na haluksy Bunito Duo — 1 UDI-DI variant, MDR

MD Atlas
Dr Sapporo Hanna Affelt Sp. j.

Data from EUDAMED, last updated May 30, 2026

Aparat korekcyjny na haluksy Bunito Duo

5908249910BU4E2

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Dr Sapporo Hanna Affelt Sp. j.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5908249910BU4E2
Device name: Aparat korekcyjny na haluksy Bunito Duo
Device model: L / écru
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 4, 2024

Manufacturer & authorised representative

Manufacturer

Name: Dr Sapporo Hanna Affelt Sp. j.
SRN: PL-MF-000044757
Country: Poland
Email: biuro@drsapporo.com
Phone: +48566229244

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01JBVH62RCGEDZVXZ77NBRHDN3

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

Bunion Corrector Bunito Duo59082499108746