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Eluent D
EUDAMEDClass A (EU MDR)
Ref 0320200528Model 400 mL, 800 mL, 1600 mLRef 0320200507Ref 0320203006Ref 0320203005
Identity
- Trade Name
- Eluent D EUDAMED
- Device Name
- Eluent D EUDAMED
- Model / Reference
- 400 mL, 800 mL, 1600 mL EUDAMED0320200528 EUDAMED0320200507 EUDAMED0320203006 EUDAMED0320203005 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06975984065854 EUDAMED06975984060453 EUDAMED06975984066271 EUDAMED06975984066264 EUDAMED
- Basic UDI-DI
- 69703416803202041HL EUDAMED69703416803202045HU EUDAMED
- EMDN Code
- W0103010299 OTHER HAEMOGLOBIN (TYPES) TESTING - OTHER EUDAMED
Classification
- Device Class
- Class A EUDAMED
- Market of Registration
- Netherlands 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
Eluent D by Shenzhen Lifotronic Technology Co., Ltd. — 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 | 69703416803202041HL | Class A | Active |
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Manufacturer
- Manufacturer
- Shenzhen Lifotronic Technology Co., Ltd.
- EUDAMED SRN
- CN-MF-000005654
- Authorised Representative
- Umedwings Netherlands B.V. NL-AR-000000444
Sources (4)
- EUDAMED 225c60b8-3b72-4041-b154-ebc0341511be 61 fields · synced Jul 22, 2026
- EUDAMED 3cdb77e5-fd46-4120-8f2b-348763c0f4d5 61 fields · synced May 17, 2026
- EUDAMED 185fb951-0383-4f66-9679-270e1d9e23f3 61 fields · synced May 17, 2026
- EUDAMED 9260a5e7-2c5b-4e0e-ad34-95e340613c71 61 fields · synced May 19, 2026