Identity
- Trade Name
- QUANTA Flash EUDAMEDQUANTA Flash® MPO Reagents FDA UDI
- Generic Name
- Myeloperoxidase anti-neutrophil cytoplasmic antibody (MPO-ANCA) IVD, kit, chemiluminescent immunoassay FDA UDI
- Device Name
- QUANTA Flash® MPO Reagents EUDAMED1. QUANTA Flash MPO Reagent Cartridge contains the following reagents for 100 determinations: a. MPO coated paramagnetic beads, in a liquid containing buffer, protein stabilizers and preservative. b. Assay Buffer – colored pink, containing Tris-buffered saline, Tween 20, protein stabilizers and preservatives. c. Tracer IgG– Isoluminol labeled anti-human IgG antibodies, containing buffer, protein stabilizers and preservative. d. Sample Dilution Buffer – colored pink, containing Tris-buffered saline, Tween 20, protein stabilizers and preservatives. FDA UDI
- Model / Reference
- 701130 EUDAMEDFDA UDI
- Description
- 1. QUANTA Flash MPO Reagent Cartridge contains the following reagents for 100 determinations: a. MPO coated paramagnetic beads, in a liquid containing buffer, protein stabilizers and preservative. b. Assay Buffer – colored pink, containing Tris-buffered saline, Tween 20, protein stabilizers and preservatives. c. Tracer IgG– Isoluminol labeled anti-human IgG antibodies, containing buffer, protein stabilizers and preservative. d. Sample Dilution Buffer – colored pink, containing Tris-buffered saline, Tween 20, protein stabilizers and preservatives. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08426950627685 EUDAMEDFDA UDI
- Basic UDI-DI
- B-08426950627685 EUDAMED
- 510(k) Number
- K112545 FDA UDI
- FDA Product Code
- MOB FDA UDI
- EMDN Code
- W0102100402 MPO ANCA EUDAMED
- GMDN Term
- Myeloperoxidase anti-neutrophil cytoplasmic antibody (MPO-ANCA) IVD, kit, chemiluminescent immunoassay FDA UDI
Classification
- Device Class
- Class IVD General 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
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-08426950627685 | 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 edb3b12b-c425-4454-b5f6-ab0ea1792a5e 61 fields · synced May 31, 2026
- FDA UDI 3048d1eb-32f5-4aec-9abb-8a0f97520a7e 36 fields · synced May 30, 2026