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Leica Biosystems CytoVision Brightfield & FL ChromaScan upgrade
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Leica Biosystems CytoVision Brightfield & FL ChromaScan upgrade FDA UDI
- Generic Name
- Laboratory instrument/analyser application software IVD FDA UDI
- Device Name
- Leca Biosystems CytoVision Brightfield & FL ChromaScan upgrade FDA UDI
- Model / Reference
- 23MBX008KFXUPG FDA UDI
- Description
- Leca Biosystems CytoVision Brightfield & FL ChromaScan upgrade FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00849832003779 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Leica Biosystems CytoVision Brightfield & FL ChromaScan 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 9a1e60fd-ae16-419f-968f-17f07a378910 37 fields · synced May 30, 2026