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SW Acquisition New User (Navios EX)

EUDAMEDFDA UDI

Class A (EU MDR)

Ref B91237Model Navios EX Instrument & Software

by Beckman Coulter Ireland Inc.

Identity

Trade Name
SW Acquisition New User (Navios EX) EUDAMED
Navios EX FDA UDI
Generic Name
Laboratory instrument/analyser application software IVD FDA UDI
Device Name
Navios EX Instrument & Software EUDAMED
NAVIOS EX ACQUISITION NEW USER SOFTWARE V2.0 WIN 7 FDA UDI
Model / Reference
Navios EX Instrument & Software EUDAMED
B91237 EUDAMED
ACQUISITION NEW USER SOFTWARE V2.0 WIN 7 FDA UDI
Description
NAVIOS EX ACQUISITION NEW USER SOFTWARE V2.0 WIN 7 FDA UDI

Identifiers

Catalog Number
B91237 FDA UDI
Primary DI / UDI-DI
15099590683245 EUDAMEDFDA UDI
Basic UDI-DI
150995902LSFlowCytomet8B EUDAMED
510(k) Number
K162897 FDA UDI
FDA Product Code
OYE FDA UDI
EMDN Code
W0202040182 CYTOFLOWMETERS - SOFTWARE ACCESSORIES EUDAMED
GMDN Term
Laboratory instrument/analyser application software IVD FDA UDI

Classification

Device Class
Class A EUDAMED
Class II FDA UDI
Regulation Number
864.5220 FDA UDI
Special Device Type
Software EUDAMED
Market of Registration
Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

SW Acquisition New User (Navios EX) by Beckman Coulter Ireland 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
IE-MF-000000887

Sources (2)

  • EUDAMED 66d3eff1-ec5b-4ead-b576-f3020005a107 61 fields · synced Oct 6, 2026
  • FDA UDI 4d1ebc53-7c01-41ab-ab1c-07b937dd6dac 35 fields · synced May 30, 2026