GUDIDData
eudamed_udi Primary ID: 03700546710407

Withings BeamO companion app (UDI 03700546710407)

Manufactured by Withings

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Withings BeamO companion app - Primary ID 03700546710407

Device Regulatory Overview

The Withings BeamO companion app (Model/Catalog Number: SCT-CPN) is a medical device manufactured by Withings. This product is indexed under FDA Product Code / Category Classification Z1203020282 within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 1 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-1280-2023 View Full Alert →

Scan Monitor/ScanWatch, model number hwa09 Wearable, Bluetooth-connected wrist watch that records heart activity (ECG) and oxygen saturat...

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Technical Specifications

Model Number
SCT-CPN
Product Code / EMDN
Z1203020282
Device Name
Withings BeamO companion app
Database Sync Date
2026-08-09 17:38:12

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Withings BeamO companion app?

The registered manufacturer of record for Withings BeamO companion app is Withings.

What is the Primary UDI-DI identifier for Withings BeamO companion app?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03700546710407.

What classification code is assigned to this device?

This device is registered under product classification code Z1203020282.

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