Identity
- Trade Name
- Leica Biosystems CytoVision OBJ HC PL APO 10X FDA UDI
- Generic Name
- Microscope objective FDA UDI
- Device Name
- Leica Biosystems CytoVision OBJ HC PL APO 10X FDA UDI
- Model / Reference
- 23OBJ010PAPDRY FDA UDI
- Description
- Leica Biosystems CytoVision OBJ HC PL APO 10X FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00849832009375 FDA UDI
- FDA Product Code
- JOY FDA UDI
- GMDN Term
- Microscope objective 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 OBJ HC PL APO 10X by Leica Biosystems Richmond, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 30f99b99-22f2-4e2d-a755-0142b4052b7a 37 fields · synced Jun 8, 2026