Duns Number:063519193
Device Description: Probe Covers Clear Polyethylene Sterile 9in x 96in x 1 in, 100 per Case
Catalog Number
-
Brand Name
Abbott Medical
Version/Model Number
33442
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
September 21, 2022
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"
Yes
For Single-Use
Yes
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
KKX
Product Code Name
Drape, Surgical
Public Device Record Key
401bba3a-7526-41a7-a362-8f093779d577
Public Version Date
September 22, 2022
Public Version Number
3
DI Record Publish Date
October 04, 2017
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 | 222 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 2255 |