ThinPrep Imaging System - Hologic, Inc.

Duns Number:018925968

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More Product Details

Catalog Number

CMP-01667

Brand Name

ThinPrep Imaging System

Version/Model Number

ThinPrep Imaging System Workstation

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

October 31, 2025

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)

-

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

MNM

Product Code Name

READER, CERVICAL CYTOLOGY SLIDE, AUTOMATED

Device Record Status

Public Device Record Key

ec950ee4-bc6e-4db4-ba59-2756a8857fca

Public Version Date

March 22, 2022

Public Version Number

3

DI Record Publish Date

December 03, 2019

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"HOLOGIC, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 130
2 A medical device with a moderate to high risk that requires special controls. 311
3 A medical device with high risk that requires premarket approval 96