Identity
- Trade Name
- Nokia FDA UDI
- Generic Name
- Bioelectrical body composition analyser FDA UDI
- Model / Reference
- WBS04-Black FDA UDI
Identifiers
- Primary DI / UDI-DI
- 03700546702341 FDA UDI
- FDA Product Code
- FRI FDA UDIPUH FDA UDI
- GMDN Term
- Bioelectrical body composition analyser FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.2700 FDA UDI870.2770 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Bioelectrical body composition analyser
Nokia by Withings SA — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bioelectrical body composition analyser.
- TANITA Body Composition Analyzer — Tanita Corp. · Class II
- Beurer — BEURER NORTH AMERICA, L.P. · Class II
- Imp SFB7 — IMPEDIMED, INC. · Class II
- CONAIR — CONAIR LLC. · Class II
- RENPHO Body Composition Scale — JOICOM CORPORATION · Class II
- Etekcity — ETEKCITY CORPORATION · Class II
- truME — Shenzhen Belter Health Measurement and Analysis Technology Co., Ltd. · Class II
- CONAIR — CONAIR LLC. · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Withings SA
Sources (1)
- FDA UDI 255b82d1-39d0-46ed-af51-f9d7432e72ac 32 fields · synced Jun 8, 2026