Identity
- Trade Name
- LIAISON XL MUREX HIV Ab/Ag HT FDA UDI
- Generic Name
- HIV1/HIV2 antigen/antibody IVD, kit, chemiluminescent immunoassay FDA UDI
- Model / Reference
- 318290 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08056771500203 FDA UDI
- GMDN Term
- HIV1/HIV2 antigen/antibody IVD, kit, chemiluminescent immunoassay FDA UDI
Classification
- 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
No
FDA UDI
Category: HIV1/HIV2 antigen/antibody IVD, kit, chemiluminescent immunoassay
LIAISON XL MUREX HIV Ab/Ag HT by Diasorin S.P.A — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as HIV1/HIV2 antigen/antibody IVD, kit, chemiluminescent immunoassay.
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- Elecsys HIV combi PT — Roche Diagnostics Corp. · Class II
- ARCHITECT — Abbott · Class II
- Elecsys HIV Duo — Roche Diagnostics Corp. · 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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Diasorin S.P.A
Sources (1)
- FDA UDI 12672edb-595b-43af-a9e4-8ef954b4ed39 32 fields · synced May 29, 2026