Identity
- Trade Name
- Aptiva® APS IgG Reagent EUDAMEDFDA UDI
- Generic Name
- Anticardiolipin antibody IVD, kit, fluorescent immunoassay FDA UDI
- Device Name
- Aptiva® APS IgG Reagent EUDAMED1. Aptiva APS IgG Reagent Cartridge -APS IgG Beads (1x0.5mL) -Assay Buffer (1x17mL) -PE Tracer IgG(1x17mL) -Rehydration Buffer (1x6.5mL) FDA UDI
- Model / Reference
- 725100 EUDAMEDFDA UDI
- Description
- 1. Aptiva APS IgG Reagent Cartridge -APS IgG Beads (1x0.5mL) -Assay Buffer (1x17mL) -PE Tracer IgG(1x17mL) -Rehydration Buffer (1x6.5mL) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08430793040716 EUDAMEDFDA UDI
- Basic UDI-DI
- 84307930407163S EUDAMED
- 510(k) Number
- K223093 FDA UDI
- FDA Product Code
- MID FDA UDIMSV FDA UDI
- EMDN Code
- W0102100501,W0102100503 EUDAMED
- GMDN Term
- Anticardiolipin antibody IVD, kit, fluorescent immunoassay FDA UDI
Classification
- Device Class
- Class B EUDAMEDClass II FDA UDI
- Regulation Number
- 866.5660 FDA UDI
- Market of Registration
- Italy EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Human Tissues
Yes
EUDAMED
Animal Tissues
Yes
EUDAMED
Microbial Substances
No
EUDAMED
Reagent
Yes
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
New Device
Yes
EUDAMED
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
Aptiva® APS IgG Reagent by Inova Diagnostics, Inc. — Class B — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/IVDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 84307930407163S | Class B | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class B | Pending data |
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Manufacturer
- Manufacturer
- Inova Diagnostics. Inc.
- EUDAMED SRN
- US-MF-000017851
- Authorised Representative
- Medical Technology Promedt Consulting GmbH DE-AR-000000085
Sources (2)
- EUDAMED 8392a912-6e86-43b1-acc0-9e86ae8356e7 61 fields · synced May 30, 2026
- FDA UDI d9cc4830-7ceb-4245-a0c5-04a9e7ba9a9e 36 fields · synced May 30, 2026