Identity
- Trade Name
- Sunquest VUE FDA UDI
- Generic Name
- Pathology information system application software FDA UDI
- Device Name
- Sunquest VUE supports laboratories in the management of patient reports and to transfer, store, and display test results and information. FDA UDI
- Model / Reference
- 3.0 FDA UDI
- Description
- Sunquest VUE supports laboratories in the management of patient reports and to transfer, store, and display test results and information. FDA UDI
Identifiers
- Primary DI / UDI-DI
- B236VUE3000 FDA UDI
- FDA Product Code
- OUG FDA UDI
- GMDN Term
- Pathology information system application software FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6310 FDA UDI
- Commercial Distribution
- Not 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
No
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Sunquest VUE by CliniSys, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- CliniSys, Inc
Sources (1)
- FDA UDI 08846855-58b6-4165-825f-799a10ca7e30 34 fields · synced May 30, 2026