Identity
- Trade Name
- UbiqVue FDA UDI
- Generic Name
- Wireless patient monitor/sensor reporting software, professional-only FDA UDI
- Device Name
- Holter Web Portal FDA UDI
- Model / Reference
- UA2251-C FDA UDI
- Description
- Holter Web Portal FDA UDI
Identifiers
- Primary DI / UDI-DI
- B353UA2251C1 FDA UDI
- FDA Product Code
- DRG FDA UDI
- GMDN Term
- Wireless patient monitor/sensor reporting software, professional-only FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2910 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
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Category: Wireless patient monitor/sensor reporting software, professional-only
UbiqVue by LifeSignals, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Wireless patient monitor/sensor reporting software, professional-only.
- LEAF™ — Smith & Nephew Medical, Ltd. · Class I
- Atlas Sensor — ATLAS LIFT TECH, INC. · Class I
- LEAF™ — Smith & Nephew Medical, Ltd. · Class I
- UbiqVue — LifeSignals, Inc. · 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 II | Pending data |
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Manufacturer
- Manufacturer
- LifeSignals, Inc.
Sources (1)
- FDA UDI 4957f96f-316b-4b43-897c-dcbc2906e1a3 34 fields · synced Jun 7, 2026