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ST AIA-PACK Myoglobin SAMPLE DILUTING SOLUTION
EUDAMEDFDA UDIClass IVD General (EU MDR)
Ref 0025597
Identity
- Trade Name
- ST AIA-PACK Myoglobin SAMPLE DILUTING SOLUTION FDA UDI
- Generic Name
- Myoglobin IVD, reagent FDA UDI
- Device Name
- ST AIA-PACK Myoglobin SAMPLE DILUTING SOLUTION EUDAMED
- Model / Reference
- 0025597 EUDAMEDN/A FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04560189211025 EUDAMEDFDA UDI
- Basic UDI-DI
- B-04560189211025 EUDAMED
- FDA Product Code
- DDR FDA UDI
- EMDN Code
- W01021304 MYOGLOBIN EUDAMED
- GMDN Term
- Myoglobin IVD, reagent FDA UDI
Classification
- Device Class
- Class IVD General EUDAMEDClass II FDA UDI
- Regulation Number
- 866.5680 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
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
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
ST AIA-PACK Myoglobin SAMPLE DILUTING SOLUTION by Tosoh Corporation — Class IVD General — IVDD, FDA UDI — listed in EUDAMED, FDA GUDID
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-04560189211025 | 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 9f187ff9-5672-4a24-a852-13c5432e5767 61 fields · synced Jun 18, 2026
- FDA UDI 9c509696-9842-4fbe-8f3c-578d2531c823 34 fields · synced May 29, 2026