Duns Number:012925513
Device Description: 3 INCH SELF SEAL POUCH (0033)
Catalog Number
-
Brand Name
3 INCH SELF SEAL POUCH (0033)
Version/Model Number
01I0033
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K870147
Product Code
FRG
Product Code Name
Wrap, Sterilization
Public Device Record Key
7d1825d3-e883-49a0-9300-c8c985fa2a2f
Public Version Date
November 08, 2019
Public Version Number
4
DI Record Publish Date
September 12, 2016
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 130 |