Duns Number:018925968
Catalog Number
CMP-01764
Brand Name
Thinprep Imaging System
Version/Model Number
Thinprep Imaging System Computer
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
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
MNM
Product Code Name
READER, CERVICAL CYTOLOGY SLIDE, AUTOMATED
Public Device Record Key
d959b79f-4d6f-4527-9622-4cdc9f085c75
Public Version Date
March 22, 2022
Public Version Number
2
DI Record Publish Date
June 24, 2020
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
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 |