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Dako Fluorescence Mounting Medium
EUDAMEDClass A (EU MDR)
Ref S3023Model S302380-2
Identity
- Trade Name
- Dako Fluorescence Mounting Medium EUDAMED
- Device Name
- Dako Fluorescence Mounting Medium EUDAMED
- Model / Reference
- S302380-2 EUDAMEDS3023 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05700571104699 EUDAMED
- Basic UDI-DI
- 570057P3007P3010A053801PE EUDAMED
- EMDN Code
- W01030708 STAIN SOLUTIONS (HISTOLOGY/CYTOLOGY) EUDAMED
Classification
- Device Class
- Class A EUDAMED
- Market of Registration
- Denmark EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Microbial Substances
No
EUDAMED
Reagent
Yes
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
New Device
No
EUDAMED
Dako Fluorescence Mounting Medium by Agilent Technologies 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 | 570057P3007P3010A053801PE | Class A | Active |
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Manufacturer
- Manufacturer
- Agilent Technologies, Inc.
- EUDAMED SRN
- US-MF-000009385
- Authorised Representative
- Agilent Technologies Denmark ApS DK-AR-000001443
Sources (1)
- EUDAMED f7bfb7fa-226f-42ef-a5ff-df3eee0a6924 61 fields · synced Jul 31, 2026