Duns Number:008124539
Device Description: Non-Woven IV Sponge, 2"x2", 6-ply, Sterile, 2'ss.
Catalog Number
-
Brand Name
Non-Woven IV Sponge
Version/Model Number
4610
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Safe
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"
Yes
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
-
Product Code
FRL
Product Code Name
Fiber, Medical, Absorbent
Public Device Record Key
6d169186-9731-4a06-b45b-d066b1f1dd1a
Public Version Date
August 24, 2021
Public Version Number
2
DI Record Publish Date
June 21, 2021
Package DI Number
00616784461021
Quantity per Package
35
Contains DI Package
00616784461014
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Box
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 694 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 226 |
| 3 | A medical device with high risk that requires premarket approval | 2 |