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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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Force Biofeedback — 3 UDI-DI variants, MDR (OT Bioelettronica srl)

MD Atlas
OT Bioelettronica srl

Data from EUDAMED, last updated May 30, 2026

Force Biofeedback

805697785NODALGDYN004PN

3 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: 805697785NODALGDYN004PN
Device name: —
Device model: Force Biofeedback
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 10, 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

3 UDI-DI variants

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Applied filters

basicUdiUlid01H02J88H92A7YKAB43FF1B3NV

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

OT023408056977851260
OT011008056977850096
OT023608056977851291