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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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Neobrush — 60 UDI-DI variants, MDR (Asept InMed)

MD Atlas
Asept InMed

Data from EUDAMED, last updated May 19, 2026

Neobrush

3660869ecouvillonsJD

60 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: Asept InMed

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3660869ecouvillonsJD
Device name: Neobrush
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: Asept InMed
SRN: FR-MF-000009405
Country: France
Email: fmeghelli@aseptinmed.fr
Phone: +33 5 31 22 44 90

Variants by status

UDI-DI variants

60 UDI-DI variants

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Applied filters

basicUdiUlid01KFJH6J0FQ8XTV72VTV298HNP

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

Neobrush03660869017778
Neobrush03660869016887
Neobrush03660869016832
Neobrush03660869016603
Neobrush03660869016856
Neobrush03660869016788
Neobrush03660869016795
Neobrush03660869016610
Neobrush03660869017136
22227403660869222745

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