Duns Number:011005491
Device Description: Pediatric Intermittent Catheter, Coude-tip
Catalog Number
-
Brand Name
MTG Pediatric Intermittent Catheter, Coude-tip
Version/Model Number
71608
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
K111405,K111405,K111405
Product Code
GBM
Product Code Name
Catheter, Urethral
Public Device Record Key
7b77a682-ef86-4759-99ef-7716d118aa4c
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
September 13, 2016
Package DI Number
20851593006252
Quantity per Package
12
Contains DI Package
10851593006255
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 1 |
2 | A medical device with a moderate to high risk that requires special controls. | 121 |