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Leica Biosystems CytoVision Karyotyping Software Upgrade
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Leica Biosystems CytoVision Karyotyping Software Upgrade FDA UDI
- Generic Name
- Laboratory instrument/analyser application software IVD FDA UDI
- Device Name
- Leica Biosystems CytoVision Karyotyping Software Upgrade FDA UDI
- Model / Reference
- 23SWR001KLX001 FDA UDI
- Description
- Leica Biosystems CytoVision Karyotyping Software Upgrade FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00849832003670 FDA UDI
- FDA Product Code
- JOY FDA UDI
- GMDN Term
- Laboratory instrument/analyser application software IVD FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.5260 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
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Leica Biosystems CytoVision Karyotyping Software Upgrade by Leica Biosystems Richmond, Inc. — Class II — FDA UDI — listed in FDA GUDID
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
- Leica Biosystems Richmond, Inc.
Sources (1)
- FDA UDI 7407f709-a6c7-4084-9cb4-829c0b866fd2 37 fields · synced May 31, 2026