Identity
- Trade Name
- Direct TIBC Calibrators FDA UDI
- Generic Name
- Total iron binding capacity (TIBC) IVD, calibrator FDA UDI
- Device Name
- For calibrating the quantitative Direct Total Iron-Binding Capacity (TIBC) assay on automated chemistry analyzer systems. 2 x 1ml. FDA UDI
- Model / Reference
- TIBCC480 FDA UDI
- Description
- For calibrating the quantitative Direct Total Iron-Binding Capacity (TIBC) assay on automated chemistry analyzer systems. 2 x 1ml. FDA UDI
Identifiers
- Catalog Number
- TIBCC480 FDA UDI
- Primary DI / UDI-DI
- 00817439021274 FDA UDI
- FDA Product Code
- JIT FDA UDI
- GMDN Term
- Total iron binding capacity (TIBC) IVD, calibrator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1150 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
Direct TIBC Calibrators by Medtest DX — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Medtest DX
Sources (1)
- FDA UDI 38b43a9f-73a4-4b35-ab2d-40cd21226cae 37 fields · synced May 31, 2026