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Navios

FDA UDI

Class II (US FDA UDI)

by Beckman Coulter Ireland Inc.

Identity

Trade Name
Navios FDA UDI
Generic Name
Flow cytometry analyser IVD, semi-automated FDA UDI
Device Name
Navios Flow Cytometer FDA UDI
Model / Reference
6 Color 2 lasers FDA UDI
Description
Navios Flow Cytometer FDA UDI

Identifiers

Catalog Number
A52101 FDA UDI
Primary DI / UDI-DI
15099590514730 FDA UDI
FDA Product Code
OYE FDA UDI
GMDN Term
Flow cytometry analyser IVD, semi-automated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.5220 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Category: Flow cytometry analyser IVD, semi-automated

Navios by Beckman Coulter Ireland Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flow cytometry analyser IVD, semi-automated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Beckman Coulter Ireland Inc.

Sources (1)

  • FDA UDI 106a3593-dce3-4787-8e97-5dd922cc3c2f 34 fields · synced May 29, 2026