Identity
- Trade Name
- STA® - Liatest® VWF:Ag FDA UDI
- Generic Name
- Coagulation factor VIII-associated antigen IVD, kit, nephelometry/turbidimetry FDA UDI
- Model / Reference
- 00518 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 03607450005189 FDA UDI
- 510(k) Number
- K962675 FDA UDI
- FDA Product Code
- GJT FDA UDI
- GMDN Term
- Coagulation factor VIII-associated antigen IVD, kit, nephelometry/turbidimetry FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.7290 FDA UDI
- Commercial Distribution
- 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
Yes
FDA UDI
Category: Coagulation factor VIII-associated antigen IVD, kit, nephelometry/turbidimetry
STA® - Liatest® VWF:Ag by Diagnostica Stago, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Coagulation factor VIII-associated antigen IVD, kit, nephelometry/turbidimetry.
- vWF Ag — SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD · Class II
- vWF Ag — SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD · Class II
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
- Diagnostica Stago, Inc.
Sources (1)
- FDA UDI 7b49f809-0b5a-44b9-8518-5cb07042956c 34 fields · synced Jun 1, 2026