Identity
- Trade Name
- LIAISON XL MUREX Anti-HBe FDA UDI
- Generic Name
- Hepatitis B virus e-antigen total antibody IVD, kit, chemiluminescent immunoassay FDA UDI
- Model / Reference
- 318160 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08056771103428 FDA UDI
- GMDN Term
- Hepatitis B virus e-antigen total 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: Hepatitis B virus e-antigen total antibody IVD, kit, chemiluminescent immunoassay
LIAISON XL MUREX Anti-HBe by Diasorin Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Hepatitis B virus e-antigen total antibody IVD, kit, chemiluminescent immunoassay.
- Atellica IM aHBe2 — Siemens Healthcare Diagnostics · Class II
- VITROS — Ortho-Clinical Diagnostics · Class II
- Elecsys Anti-HBe — Roche Diagnostics Corp. · Class II
- ADVIA Centaur aHBe2 50T Kit — Siemens Healthcare Diagnostics · Class II
- VITROS — Ortho-Clinical Diagnostics · 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 Inc.
Sources (1)
- FDA UDI 9edf36d9-082f-4193-a4c1-d3a43c0b9521 32 fields · synced May 31, 2026