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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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ENDOBRUSH — 3 UDI-DI variants, MDR (BIOGYN SRL)

MD Atlas
BIOGYN SRL

Data from EUDAMED, last updated May 31, 2026

ENDOBRUSH

805697735000JG

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: BIOGYN SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805697735000JG
Device name: ENDOBRUSH
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: BIOGYN SRL
SRN: IT-MF-000033403
Country: Italy
Email: biogyn@biogyn.it
Phone: +39 0535 26889

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KKKW5KZ2CQM45DMSBEQ7KTYM

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

ENDOBRUSH18056977352177
EBR1 N2518056977352160
PLASTIC SPATULA18056977352184