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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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Accessories — 10 UDI-DI variants, MDR (OT Bioelettronica srl)

MD Atlas
OT Bioelettronica srl

Data from EUDAMED, last updated May 30, 2026

Accessories

805697785MECHPART007J6

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: OT Bioelettronica srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805697785MECHPART007J6
Device name: —
Device model: Accessories
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 20, 2023

Manufacturer & authorised representative

Manufacturer

Name: OT Bioelettronica srl
SRN: IT-MF-000033348
Country: Italy
Email: a.bottin@otbioelettronica.it
Phone: +3901119720518

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01H3BWR50VFNVM1GKHR2ZSZCZ7

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

OT017608056977850621
OT028708056977852038
OT032008056977852540
OT032108056977852557
OT018708056977850683
OT017708056977850652
OT018108056977850591
OT018208056977850607
OT017808056977850669
OT029108056977852045