Duns Number:109903521
Device Description: BOOT INSERT PAD
Catalog Number
72200635
Brand Name
NA
Version/Model Number
72200635
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
Yes
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
KQZ
Product Code Name
COMPONENT, TRACTION, NON-INVASIVE
Public Device Record Key
a4a192c0-9816-4fc4-bca5-40ea286a8cae
Public Version Date
October 07, 2020
Public Version Number
4
DI Record Publish Date
August 29, 2015
Package DI Number
23596010578130
Quantity per Package
2
Contains DI Package
03596010578136
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
BX
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 10651 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 35590 |
| 3 | A medical device with high risk that requires premarket approval | 351 |