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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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Withings BeamO — 2 UDI-DI variants, MDR (Withings)

MD Atlas
Withings

Data from EUDAMED, last updated May 19, 2026

Withings BeamO

3700546709937X2

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Withings

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Device characteristics

Active deviceMeasuring function

Clinical investigations

Investigation number: 2024-A00759-38
Registered: No
Countries: United States

Registered: No

Investigation number: HLSZU20241010
Registered: No
Countries: China

Investigation number: NCT06637878
Registered: No
Countries: United States

Identity & classification

Basic UDI-DI: 3700546709937X2
Device name: Withings BeamO
Device model: SCT02
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 11, 2025

Manufacturer & authorised representative

Manufacturer

Name: Withings
SRN: FR-MF-000009505
Country: France
Email: regulatory@withings.com
Phone: +33141460460

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JRJF78S8YJJ3S2B2K2XC53DT

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

SCT02-0303700546709937
SCT02-0203700546710209