Identity
- Trade Name
- LIAISON® LH FDA UDI
- Generic Name
- Luteinizing hormone (LH) IVD, kit, chemiluminescent immunoassay FDA UDI
- Model / Reference
- 312201 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08056771200134 FDA UDI
- GMDN Term
- Luteinizing hormone (LH) 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
No
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: Luteinizing hormone (LH) IVD, kit, chemiluminescent immunoassay
Liaison® Lh by Diasorin Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Luteinizing hormone (LH) IVD, kit, chemiluminescent immunoassay.
- ADVIA Centaur® LH — Siemens Healthcare Diagnostics · Class I
- Alinity — ABBOTT IRELAND · Class I
- Elecsys LH — Roche Diagnostics Corp. · Class I
- ADVIA Centaur® LH — Siemens Healthcare Diagnostics · Class I
- VITROS — Ortho-Clinical Diagnostics · Class I
- Alinity — ABBOTT IRELAND · Class I
- IMMULITE® 2000 Systems LH — SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD · Class I
- Dimension Vista® Flex® reagent cartridge LH — Siemens Healthcare Diagnostics · Class I
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 0c9d48ef-0b24-496f-a380-61e97c0e7281 33 fields · synced Jun 8, 2026