Identity
- Trade Name
- LIAISON Q.S.E.T. Device Plus FDA UDI
- Generic Name
- Calprotectin IVD, reagent FDA UDI
- Device Name
- Fecal extraction device FDA UDI
- Model / Reference
- 319060 FDA UDI
- Description
- Fecal extraction device FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08056771602884 FDA UDI
- 510(k) Number
- K213858 FDA UDI
- FDA Product Code
- NXO FDA UDI
- GMDN Term
- Calprotectin IVD, reagent FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 866.5180 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
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: Calprotectin IVD, reagent
LIAISON Q.S.E.T. Device Plus by Diasorin Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 | Class II | Pending data |
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Manufacturer
- Manufacturer
- Diasorin Inc.
Sources (1)
- FDA UDI 137cca98-5846-4fec-bbb2-a01a52db8d9e 34 fields · synced May 31, 2026