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Aia-Pack Fer Sample Diluting Solution
EUDAMEDFDA UDIClass IVD General (EU MDR)
Ref 0020553
Identity
- Trade Name
- AIA-PACK FER Sample Diluting Solution FDA UDI
- Generic Name
- Ferritin IVD, reagent FDA UDI
- Device Name
- AIA-PACK FER SAMPLE DILUTING SOLUTION EUDAMED
- Model / Reference
- 0020553 EUDAMEDN/A FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04560189211452 EUDAMEDFDA UDI
- Basic UDI-DI
- B-04560189211452 EUDAMED
- FDA Product Code
- DBF FDA UDI
- EMDN Code
- W0102070102 FERRITIN EUDAMED
- GMDN Term
- Ferritin IVD, reagent FDA UDI
Classification
- Device Class
- Class IVD General EUDAMEDClass II FDA UDI
- Regulation Number
- 866.5340 FDA UDI
- Market of Registration
- Belgium EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Human Tissues
Yes
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
Prescription Use
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Aia-Pack Fer Sample Diluting Solution by Tosoh Corporation — Class IVD General — IVDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/IVDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDD | B-04560189211452 | Class IVD General | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IVD General | Pending data |
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Manufacturer
- Manufacturer
- Tosoh Corporation
- EUDAMED SRN
- JP-MF-000024143
- Authorised Representative
- Tosoh Europe N.V. BE-AR-000000211
Sources (2)
- EUDAMED b6e46615-0a45-4db8-aac0-a699910b95f1 61 fields · synced Jul 9, 2026
- FDA UDI b9787032-1e61-450f-8573-5e555bc66db7 34 fields · synced May 30, 2026