Identity
- Trade Name
- Triage FDA UDI
- Generic Name
- Placental growth factor (PLGF) IVD, kit, fluorescent immunoassay FDA UDI
- Device Name
- Triage PLGF Test (OUS) FDA UDI
- Model / Reference
- 98800EU FDA UDI
- Description
- Triage PLGF Test (OUS) FDA UDI
Identifiers
- Catalog Number
- 98800EU FDA UDI
- Primary DI / UDI-DI
- 30014613338048 FDA UDI
- FDA Product Code
- PZN FDA UDI
- GMDN Term
- Placental growth factor (PLGF) IVD, kit, fluorescent immunoassay FDA UDI
Classification
- Device Class
- N 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
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
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Placental growth factor (PLGF) IVD, kit, fluorescent immunoassay
Triage by Quidel Cardiovascular Inc. — Class N — 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 | Class N | Pending data |
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Manufacturer
- Manufacturer
- Quidel Cardiovascular Inc.
Sources (1)
- FDA UDI fc4ad048-71c9-44d2-bb24-cbd5bc853e57 35 fields · synced Jun 6, 2026