← Back to catalogue
EliA Sample Diluent
EUDAMEDFDA UDIClass A (EU MDR)
Ref 83-1144-01Ref 83-1023-01
by Phadia AB
Identity
- Trade Name
- EliA Sample Diluent EUDAMEDFDA UDI
- Generic Name
- Plasma protein IVD, reagent FDA UDI
- Device Name
- Sample Diluent EUDAMEDEliA Sample Diluent FDA UDI
- Model / Reference
- 83-1144-01 EUDAMED83-1023-01 EUDAMED83-0003-71 FDA UDI
- Description
- EliA Sample Diluent FDA UDI
Identifiers
- Catalog Number
- 83-0003-71 FDA UDI
- Primary DI / UDI-DI
- 07333066016207 EUDAMED07333066012872 EUDAMEDFDA UDI
- Basic UDI-DI
- 7333066BUDI0003LL EUDAMED
- FDA Product Code
- NHX FDA UDI
- EMDN Code
- W01029003 BUFFERS (UNASSIGNABLE), SUPPLEM. REAGENTS, ETC (IC) EUDAMED
- GMDN Term
- Plasma protein IVD, reagent FDA UDI
Classification
- Device Class
- Class A EUDAMEDClass II FDA UDI
- Regulation Number
- 866.5775 FDA UDI
- Market of Registration
- Sweden EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Human Tissues
No
EUDAMED
Animal Tissues
Yes
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
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
EliA Sample Diluent by Phadia AB — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/IVDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 7333066BUDI0003LL | Class A | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class A | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Phadia AB
- EUDAMED SRN
- SE-MF-000014170
Sources (3)
- EUDAMED b84c289e-b9fc-4f4e-b61e-c258fe104833 61 fields · synced Aug 4, 2026
- EUDAMED 4b8a2906-17a7-4024-ba49-bea9af41d7c9 61 fields · synced May 18, 2026
- FDA UDI 1feb7389-84b3-4770-a399-9253f85e0153 36 fields · synced May 30, 2026