Leica Biosystems CytoVision DM6000B for Brightfield & FL - Leica Biosystems CytoVision DM6000B for - Leica Biosystems Richmond, Inc.

Duns Number:082930884

Device Description: Leica Biosystems CytoVision DM6000B for Brightfield & FL

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More Product Details

Catalog Number

-

Brand Name

Leica Biosystems CytoVision DM6000B for Brightfield & FL

Version/Model Number

23MIC600KFX002

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code Details

Product Code

JOY

Product Code Name

DEVICE, AUTOMATED CELL-LOCATING

Device Record Status

Public Device Record Key

dbf9136d-0ed6-442e-a243-55eee4eb1624

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 17, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"LEICA BIOSYSTEMS RICHMOND, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 4
2 A medical device with a moderate to high risk that requires special controls. 206