Identity
- Trade Name
- Xeleris Processing and Review Workstation FDA UDI
- Generic Name
- Nuclear medicine system workstation FDA UDI
- Device Name
- Xeleris V Clinical Application SW FDA UDI
- Model / Reference
- V FDA UDI
- Description
- Xeleris V Clinical Application SW FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00195278245021 FDA UDI
- 510(k) Number
- K201103 FDA UDI
- FDA Product Code
- LLZ FDA UDI
- GMDN Term
- Nuclear medicine system workstation 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
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Nuclear medicine system workstation
Xeleris Processing and Review Workstation by Ge Medical Systems Israel , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Xeleris Processing and Review Workstation — Ge Medical Systems Israel , Ltd. · Class II
- Xeleris Processing and Review System — Ge Medical Systems Israel , Ltd. · Class II
- Xeleris Processing and Review Workstation — Ge Medical Systems Israel , Ltd. · 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
- Ge Medical Systems Israel , Ltd.
Sources (1)
- FDA UDI 245b99d3-9026-4fd7-831f-a10230c139af 34 fields · synced Jun 1, 2026