Duns Number:006261481
Device Description: INTRDCR 050011 5PK 5F 11CM INPT INTR KIT
Catalog Number
-
Brand Name
INPUT™ PS
Version/Model Number
050011
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
K132617,K132617
Product Code
DYB
Product Code Name
INTRODUCER, CATHETER
Public Device Record Key
0a6096a4-c2f3-4e1e-a7f6-8f4b3505ce78
Public Version Date
June 07, 2019
Public Version Number
4
DI Record Publish Date
February 02, 2017
Package DI Number
20643169014330
Quantity per Package
5
Contains DI Package
00643169014336
Package Discontinue Date
-
Package Status
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 |