Identity
- Trade Name
- QUANTA Flash EUDAMEDQUANTA Flash® aCL IgG Controls FDA UDI
- Generic Name
- Anticardiolipin antibody IVD, control FDA UDI
- Device Name
- QUANTA Flash® aCL IgG Controls EUDAMED1. QUANTA Flash aCL IgG Low Control 3 x 1 mL barcoded tubes of a solution with aCL IgG in saline solution containing fetal bovine serum stabilizers and preservative. 2. QUANTA Flash aCL IgG High Control 3 x 1 mL barcoded tubes of a solution with aCL IgG in saline solution containing fetal bovine serum, stabilizers and preservative. FDA UDI
- Model / Reference
- 701232 EUDAMEDFDA UDI
- Description
- 1. QUANTA Flash aCL IgG Low Control 3 x 1 mL barcoded tubes of a solution with aCL IgG in saline solution containing fetal bovine serum stabilizers and preservative. 2. QUANTA Flash aCL IgG High Control 3 x 1 mL barcoded tubes of a solution with aCL IgG in saline solution containing fetal bovine serum, stabilizers and preservative. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08426950554486 EUDAMEDFDA UDI
- Basic UDI-DI
- B-08426950554486 EUDAMED
- 510(k) Number
- K092181 FDA UDI
- FDA Product Code
- JJX FDA UDI
- EMDN Code
- W0102152004 CARDIAC MARKER CONTROLS EUDAMED
- GMDN Term
- Anticardiolipin antibody IVD, control FDA UDI
Classification
- Device Class
- Class IVD General EUDAMEDClass I FDA UDI
- Regulation Number
- 862.1660 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
No
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
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
QUANTA Flash by Inova Diagnostics, Inc. — Class IVD General — IVDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/IVDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDD | B-08426950554486 | Class IVD General | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IVD General | 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 d6ddbbb3-1699-40f1-a680-66c705505835 61 fields · synced Jul 8, 2026
- FDA UDI 7475ca97-c881-4f60-8966-d5d0406628ce 36 fields · synced May 30, 2026