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NOVA Lite

EUDAMEDFDA UDI

Class IVD General (EU MDR)

Ref 708100

by Inova Diagnostics. Inc.

Identity

Trade Name
NOVA Lite EUDAMED
NOVA Lite® HEp-2 ANA Kit FDA UDI
Generic Name
Multiple antinuclear antibody (ANA) screening IVD, reagent FDA UDI
Device Name
NOVA Lite® HEp-2 ANA Kit EUDAMED
1. 20x Hep- 2 ANA Slide (12 well) 2. 1x 0.5mL IFA System Negative Control 3. 1x 15mL FITC IgG Conjugate 4. 1x 7mL Mounting Medium 5. 2x 25mL PBS II Concentrate (40x) 6 .1x Coverlips, 20 each 7. 1x 0.5mL ANA Titratable Pattern FDA UDI
Model / Reference
708100 EUDAMEDFDA UDI
Description
1. 20x Hep- 2 ANA Slide (12 well) 2. 1x 0.5mL IFA System Negative Control 3. 1x 15mL FITC IgG Conjugate 4. 1x 7mL Mounting Medium 5. 2x 25mL PBS II Concentrate (40x) 6 .1x Coverlips, 20 each 7. 1x 0.5mL ANA Titratable Pattern FDA UDI

Identifiers

Primary DI / UDI-DI
08426950456193 EUDAMEDFDA UDI
Basic UDI-DI
B-08426950456193 EUDAMED
510(k) Number
K880736 FDA UDI
FDA Product Code
LLL FDA UDI
EMDN Code
W0102100101 ANA SCREENING EUDAMED
GMDN Term
Multiple antinuclear antibody (ANA) screening IVD, reagent FDA UDI

Classification

Device Class
Class IVD General EUDAMED
Class II FDA UDI
Regulation Number
866.5100 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

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

NOVA Lite 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

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Manufacturer

EUDAMED SRN
US-MF-000017851
Authorised Representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Sources (2)

  • EUDAMED 491ebe88-dc74-45ae-9686-dac89257665a 61 fields · synced Jul 28, 2026
  • FDA UDI 2c637034-367d-4f44-ae97-749137aaee96 36 fields · synced May 30, 2026