Identity
- Trade Name
- UbiqVue FDA UDI
- Generic Name
- Network server FDA UDI
- Device Name
- Holter Central Server Software FDA UDI
- Model / Reference
- UA2251-S FDA UDI
- Description
- Holter Central Server Software FDA UDI
Identifiers
- Primary DI / UDI-DI
- B353UA2251S1 FDA UDI
- FDA Product Code
- DRG FDA UDI
- GMDN Term
- Network server 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: Network server
UbiqVue by LifeSignals, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Network server.
- TEK-CARE APPLIANCE SERVER, PAGE, 1 EV MON — Securitas Healthcare LLC · Class II
- TEK-CARE LINUX SERVER, DESK-MOUNT — Securitas Healthcare LLC · Class II
- ThinPrep Imaging System — Hologic, Inc. · Class III
- 3M™Filtek™ — 3M COMPANY · Class II
- 3M™Filtek™ — 3M COMPANY · Class II
- 3M™Filtek™ — 3M COMPANY · Class II
- ThinPrep Imaging System — Hologic, Inc. · Class III
- 3M™Filtek™ — 3M COMPANY · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- LifeSignals, Inc.
Sources (1)
- FDA UDI 83b4281b-3249-49d9-8cc7-6d037ca44bc9 34 fields · synced May 31, 2026