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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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Rectal thermometer — 6 UDI-DI variants, MDR (BABYMOOV GROUP)

MD Atlas
BABYMOOV GROUP

Data from EUDAMED, last updated May 19, 2026

Rectal thermometer

3661276CARE_ACCES200XX

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_ACCES200XX
Device name: Rectal thermometer
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

basicUdiUlid01GW2919CM6T4YX3R7FW4WXZPQ

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

Babymoov03661276180451
A032002SAV20003661276145757
Babymoov03661276187436
A032004SAV20003661276169920
A032003SAV20003661276159907
B03720003661276174504