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Leica Biosystems CytoVision Removable Archive Device
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Leica Biosystems CytoVision Removable Archive Device FDA UDI
- Generic Name
- Digital storage media FDA UDI
- Device Name
- Leica Biosystems Cytovision Removable Archive Device FDA UDI
- Model / Reference
- 23STR003XXX001 FDA UDI
- Description
- Leica Biosystems Cytovision Removable Archive Device FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00849832005155 FDA UDI
- FDA Product Code
- JOY FDA UDI
- GMDN Term
- Digital storage media 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 Removable Archive Device 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 3c1eca71-4eb5-4d70-b0db-d715c13d0cc4 37 fields · synced May 30, 2026