Duns Number:006261481
Device Description: INTRDCR 071102A 5PK 11CM 7F INPT TS WNDL
Catalog Number
-
Brand Name
INPUT™ TS
Version/Model Number
071102A
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
K955785,K955785
Product Code
DYB
Product Code Name
INTRODUCER, CATHETER
Public Device Record Key
54be0028-db64-4ac0-b998-a12103c61a8d
Public Version Date
June 07, 2019
Public Version Number
4
DI Record Publish Date
February 02, 2017
Package DI Number
20643169014521
Quantity per Package
5
Contains DI Package
00643169014527
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 |