Identity
- Trade Name
- LIAISON XL MUREX HBsAg Confirmatory FDA UDI
- Generic Name
- Hepatitis B virus surface antigen IVD, reagent FDA UDI
- Model / Reference
- 318110 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08056771103589 FDA UDI
- GMDN Term
- Hepatitis B virus surface antigen IVD, reagent 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: Hepatitis B virus surface antigen IVD, reagent
LIAISON XL MUREX HBsAg Confirmatory by Diasorin S.P.A — 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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Diasorin S.P.A
Sources (1)
- FDA UDI 8731fae8-4980-4670-8e71-fda0fdf33f80 32 fields · synced Jun 8, 2026