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Dako Omnis Buffer/Solvent Container 3.5 L
EUDAMEDClass A (EU MDR)
Ref GC109Model GC10930
Identity
- Trade Name
- Dako Omnis Buffer/Solvent Container 3.5 L EUDAMED
- Device Name
- Dako Omnis Buffer/Solvent Container 3.5 L EUDAMED
- Model / Reference
- GC10930 EUDAMEDGC109 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05700571112106 EUDAMED
- Basic UDI-DI
- 570057P3007P3010A051001MQ EUDAMED
- EMDN Code
- W0202059085 VARIOUS PROCESSING INSTRUMENTS FOR HYSTOLOGY / CYTOLOGY - CONSUMABLES 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
No
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 Omnis Buffer/Solvent Container 3.5 L by Agilent Technologies Singapore (International) Pte Ltd — Class A — IVDR — listed in EUDAMED
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 | 570057P3007P3010A051001MQ | Class A | Active |
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Manufacturer
- EUDAMED SRN
- SG-MF-000014448
- Authorised Representative
- Agilent Technologies Denmark ApS DK-AR-000001443
Sources (1)
- EUDAMED 577d2db9-d9b0-43da-9577-e173358fb6f9 61 fields · synced Jul 24, 2026