Duns Number:006261481
Device Description: CONNECTOR 6153 3/8X1/2 RED W/LL PRT&PLG
Catalog Number
-
Brand Name
Intersept®
Version/Model Number
6153
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
May 02, 2019
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
K891687,K891687
Product Code
KNX
Product Code Name
COLLECTOR, URINE, (AND ACCESSORIES) FOR INDWELLING CATHETER
Public Device Record Key
4e824135-dc2e-422e-a170-3214fc2e0c29
Public Version Date
September 22, 2022
Public Version Number
4
DI Record Publish Date
June 20, 2016
Package DI Number
20673978555397
Quantity per Package
20
Contains DI Package
00673978555393
Package Discontinue Date
May 02, 2019
Package Status
Not in Commercial Distribution
Package Type
PK
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 102 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 20495 |
| 3 | A medical device with high risk that requires premarket approval | 3601 |