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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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Nose Cleaner — 6 UDI-DI variants, MDR (BABYMOOV GROUP)

MD Atlas
BABYMOOV GROUP

Data from EUDAMED, last updated May 19, 2026

Nose Cleaner

3661276CARE_ACCES201XZ

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: BABYMOOV GROUP

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3661276CARE_ACCES201XZ
Device name: Nose Cleaner
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 21, 2023

Manufacturer & authorised representative

Manufacturer

Name: BABYMOOV GROUP
SRN: FR-MF-000030344
Country: France
Email: eudamed@babymoov.com

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01GW2F7GA4SS9B0VGP3WXQW3BC

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

A03220103661276164383
Babymoov03661276187443
A032007SAV20103661276180468
A032004SAV20103661276169937
A032002SAV20103661276145764
B03200403661276174382