Identity
- Trade Name
- Web Diagnostic Viewer FDA UDI
- Generic Name
- Radiological PACS software FDA UDI
- Device Name
- The Web Diagnostic Viewer is the radiologist diagnostic workstation including the clinical applications (implemented using Web technology) with similar functionality as the Desktop Diagnostic Viewer workstation. FDA UDI
- Model / Reference
- 15.X FDA UDI
- Description
- The Web Diagnostic Viewer is the radiologist diagnostic workstation including the clinical applications (implemented using Web technology) with similar functionality as the Desktop Diagnostic Viewer workstation. FDA UDI
Identifiers
- Catalog Number
- 839063 FDA UDI
- Primary DI / UDI-DI
- 00884838107588 FDA UDI
- 510(k) Number
- K240822 FDA UDI
- FDA Product Code
- LLZ FDA UDI
- GMDN Term
- Radiological PACS software FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.2050 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
Yes
FDA UDI
Category: Radiological PACS softwareRadiology picture archiving and communication system workstation
Web Diagnostic Viewer by Philips Medical Systems Nederland B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Radiology picture archiving and communication system workstation.
- WorkstationOne™ — Three Palm Software · Class II
- OTOPLAN — CAScination AG · Class II
- Nio Color 2MP LED — Barco, Inc. · Class II
- RamSoft — Ramsoft Inc · Class II
- Aline Ablation Intelligence — Mirada Medical, Ltd. · Class II
- Sectra Orthopedic Package — Sectra AB · Class II
- CHILI PACS — CHILI GmbH · Class II
- Nio Color 2MP — Barco, Inc. · Class II
Cleared under the same submission
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
- Philips Medical Systems Nederland B.V.
Sources (1)
- FDA UDI e2863b1d-7219-4788-b61e-7f70a7bd164a 35 fields · synced Sep 18, 2026