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Leica Biosystems CytoVision DM5500 for FL-Ergo Head

FDA UDI

Class II (US FDA UDI)

by Leica Biosystems Richmond, Inc.

Identity

Trade Name
Leica Biosystems CytoVision DM5500 for FL-Ergo Head FDA UDI
Generic Name
Fluorescence light microscope FDA UDI
Device Name
Leica Biosystems CytoVision DM5500 for FL-Ergo Head FDA UDI
Model / Reference
23MIC550FXX009 FDA UDI
Description
Leica Biosystems CytoVision DM5500 for FL-Ergo Head FDA UDI

Identifiers

Primary DI / UDI-DI
00849832004066 FDA UDI
FDA Product Code
JOY FDA UDI
GMDN Term
Fluorescence light microscope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.5260 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Fluorescence light microscope

Leica Biosystems CytoVision DM5500 for FL-Ergo Head by Leica Biosystems Richmond, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fluorescence light microscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Leica Biosystems Richmond, Inc.

Sources (1)

  • FDA UDI 0adcef77-f70b-4772-99bd-b77ecc5866a6 36 fields · synced Jun 8, 2026