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UbiqVue

FDA UDI

Class II (US FDA UDI)

by LifeSignals, Inc.

Identity

Trade Name
UbiqVue FDA UDI
Generic Name
Wireless patient monitor/sensor reporting software, professional-only FDA UDI
Device Name
Active Monitoring Portal FDA UDI
Model / Reference
UA2550-C FDA UDI
Description
Active Monitoring Portal FDA UDI

Identifiers

Primary DI / UDI-DI
B353UA2550C1 FDA UDI
FDA Product Code
DRG FDA UDI
FLL FDA UDI
MHX FDA UDI
DQA 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
880.2910 FDA UDI
870.1025 FDA UDI
870.2700 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
MRI Safety
MR Unsafe FDA UDI

Category: Wearable multiple vital physiological parameter monitorWireless 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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
LifeSignals, Inc.

Sources (1)

  • FDA UDI 69428d8a-3f74-4324-97a6-338b9c4694d5 34 fields · synced Jun 8, 2026