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AIA-PACK CEA Calibration Verification Test Set
FDA UDIClass II (US FDA UDI)
by Tosoh Corp.
Identity
- Trade Name
- AIA-PACK CEA Calibration Verification Test Set FDA UDI
- Generic Name
- Carcinoembryonic antigen (CEA) IVD, control FDA UDI
- Model / Reference
- N/A FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04560189212244 FDA UDI
- FDA Product Code
- DHX FDA UDI
- GMDN Term
- Carcinoembryonic antigen (CEA) IVD, control FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 866.6010 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Category: Carcinoembryonic antigen (CEA) IVD, control
AIA-PACK CEA Calibration Verification Test Set by Tosoh Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Tosoh Corp.
Sources (1)
- FDA UDI 4b13ca88-08be-4833-82cf-c4da9d1dbc9e 34 fields · synced May 30, 2026