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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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Bendaggi dita — 6 UDI-DI variants, MDR (Megapharma Ospedaliera s.r.l.)

MD Atlas
Megapharma Ospedaliera s.r.l.

Data from EUDAMED, last updated May 31, 2026

Bendaggi dita

80569779840BD0A7

6 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: Megapharma Ospedaliera s.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 80569779840BD0A7
Device name: Bendaggi dita
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 14, 2025

Manufacturer & authorised representative

Manufacturer

Name: Megapharma Ospedaliera s.r.l.
SRN: IT-MF-000010739
Country: Italy
Email: info@megapharma.it
Phone: +39 0423 538746

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01JV7PF0PC41EWAH6DY5HYHR5G

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

04BD003008056977981370
04BD002008056977981356
04BD001008056977981332
04BD0030-108056977981387
04BD0020-1 08056977981363
04BD0010-108056977981349