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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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  • MD Atlas
  • Withings

Data from EUDAMED, last updated May 19, 2026

Withings BeamO companion app

3700546710407UC

1 reference

Class IIa
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Risk category
Class IIa
Manufacturer
Withings

Device family identification

Device name
Withings BeamO companion app
Basic UDI-DI
3700546710407UC
Device model
SCT-CPN
Issuing agency
GS1
Special device type
refdata.special-mdr-device-type.software
Version date
May 23, 2025

Classification

Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Risk category
Class IIa
Status
On the market

Manufacturer

Manufacturer

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

Device characteristics

Active device

EMDN code(s)

European Medical Device Nomenclature — the EU product classifications carried across this device family's references.

  • Z1203020282Multi-parameter monitors - software accessories

References by status

References

1 reference

Export results

Applied filters

  • basicUdiUlid·01JVY3Y8M023Q38ME9S89GQGH1

Format

Summary

31 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
  • Market country
  • Issuing entity
  • 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
  • DM Atlas link
Trade nameReference / catalog numberUDI-DI codeQuantityStatus
SCT-CPNSCT-CPN037005467104071On the market