Duns Number:003687733
Device Description: EARLOOP, TUTEM- FUTURE DESIGN
Catalog Number
6055-14 FUTURE DESIGN
Brand Name
TUTEM
Version/Model Number
6055-14 FUTURE DESIGN
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
-
Product Code
FXX
Product Code Name
Mask, Surgical
Public Device Record Key
5c9234e0-7678-4a13-8757-a8dc75f108e3
Public Version Date
May 06, 2020
Public Version Number
5
DI Record Publish Date
November 03, 2016
Package DI Number
10817583020489
Quantity per Package
3000
Contains DI Package
00817583020482
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CASE
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 5 |
2 | A medical device with a moderate to high risk that requires special controls. | 17 |