Identity
- Trade Name
- STA® - Liquid Anti-Xa 4 FDA UDI
- Generic Name
- Heparin anti-Xa IVD, kit, chromogenic FDA UDI
- Model / Reference
- 00311US FDA UDI
Identifiers
- Primary DI / UDI-DI
- 03607450011784 FDA UDI
- 510(k) Number
- K111822 FDA UDI
- FDA Product Code
- KFF FDA UDI
- GMDN Term
- Heparin anti-Xa IVD, kit, chromogenic FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.7525 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: Heparin anti-Xa IVD, kit, chromogenic
STA® - Liquid Anti-Xa 4 by Diagnostica Stago, Inc. — Class II — IVDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Also classified as Heparin anti-Xa IVD, kit, chromogenic.
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Cleared under the same submission
K111822 also covers:
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
IVDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | IVDR | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Diagnostica Stago, Inc.
Sources (2)
- FDA UDI 5b40b061-8172-42ed-9506-c21a2fefcc00 34 fields · synced Jun 18, 2026
- EUDAMED 1 fields · synced Jun 3, 2026