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Leica DM 91024 AQUA
EUDAMEDClass A (EU MDR)
Ref 232FL4930272DXModel 23GSL10XBFF230DX
Identity
- Trade Name
- Leica DM 91024 AQUA EUDAMED
- Device Name
- CytoVision DX EUDAMED
- Model / Reference
- 23GSL10XBFF230DX EUDAMED232FL4930272DX EUDAMED
Identifiers
- Primary DI / UDI-DI
- 00815477021126 EUDAMED
- Basic UDI-DI
- 08498320358U EUDAMED
- Direct Marketing DI
- 00815477021126 EUDAMED
- EMDN Code
- W0202050380 LABORATORY INSTRUMENTS FOR MICROSCOPIC INVESTIGATIONS - HARDWARE ACCESSORIES EUDAMED
Classification
- Device Class
- Class A EUDAMED
- Market of Registration
- Austria EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Microbial Substances
No
EUDAMED
Reagent
No
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
Yes
EUDAMED
New Device
No
EUDAMED
Leica DM 91024 AQUA by Leica Biosystems Imaging, Inc. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 08498320358U | Class A | Active |
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Manufacturer
- Manufacturer
- Leica Biosystems Imaging, Inc.
- EUDAMED SRN
- US-MF-000020547
- Authorised Representative
- CEpartner4U NL-AR-000000111
Sources (1)
- EUDAMED 1ef16230-1ac0-48ff-b8c0-b7cebd959d06 61 fields · synced Jul 26, 2026