← Back to catalogue

Aptiva® Optical Cleaning Solution

EUDAMEDFDA UDI

Class A (EU MDR)

Ref AC1003

by Inova Diagnostics. Inc.

Identity

Trade Name
Aptiva® Optical Cleaning Solution EUDAMED
Aptiva® Optical Cleaning Solution FDA UDI
Generic Name
Instrument/analyser cleaning agent IVD FDA UDI
Device Name
Aptiva® Optical Cleaning Solution EUDAMED
The Aptiva Optical Cleaning Solution is for use on the Inova Diagnostics Aptiva Digital Multi-Analyte System to clean the instrument Optical Module (OM) FDA UDI
Model / Reference
AC1003 EUDAMEDFDA UDI
Description
The Aptiva Optical Cleaning Solution is for use on the Inova Diagnostics Aptiva Digital Multi-Analyte System to clean the instrument Optical Module (OM) FDA UDI

Identifiers

Primary DI / UDI-DI
08430793041140 EUDAMEDFDA UDI
Basic UDI-DI
84307930411402Y EUDAMED
FDA Product Code
NSU FDA UDI
EMDN Code
W01019001 BUFFERS (UNASSIGNABLE), SUPPLEM. REAGENTS, ETC (CC) EUDAMED
GMDN Term
Instrument/analyser cleaning agent IVD FDA UDI

Classification

Device Class
Class A EUDAMED
Class II FDA UDI
Regulation Number
862.2570 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

No

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

No

EUDAMED

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Aptiva® Optical Cleaning Solution by Inova Diagnostics, Inc. — Class A — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (2)

  • EUDAMED 4bcf56dc-1bdf-482b-9001-050eb0299890 61 fields · synced Jun 19, 2026
  • FDA UDI f004b7c3-58d5-4a85-ba58-083ed45252c4 35 fields · synced May 26, 2026