Duns Number:315018218
Device Description: HI-LINE XS DISP.DIAMOND BURR/GB740R D6.0
Catalog Number
GE399SU
Brand Name
HI-LINE XS
Version/Model Number
GE399SU
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
September 02, 2022
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
-
Product Code
HTT
Product Code Name
BURR, ORTHOPEDIC
Public Device Record Key
15245f2e-3a9b-413d-aaf2-6b33fd80fafa
Public Version Date
September 07, 2022
Public Version Number
2
DI Record Publish Date
April 23, 2020
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 |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 11840 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 7088 |
| 3 | A medical device with high risk that requires premarket approval | 37 |