Identity
- Trade Name
- LIAISON® N-TACT® PTH Gen II Specimen Diluent FDA UDI
- Generic Name
- Parathyroid hormone (PTH) IVD, reagent FDA UDI
- Model / Reference
- 317912 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08056771600453 FDA UDI
- GMDN Term
- Parathyroid hormone (PTH) 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
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: Parathyroid hormone (PTH) IVD, reagent
LIAISON® N-TACT® PTH Gen II Specimen Diluent by Diasorin Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Parathyroid hormone (PTH) IVD, reagent.
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Diasorin Inc.
Sources (1)
- FDA UDI 1755a961-770a-48e7-92d6-8fba3cf148ca 33 fields · synced Jun 7, 2026