Duns Number:106793995
Device Description: Spreader, T-Shaped, STERILE, PS, Individually Wrapped
Catalog Number
-
Brand Name
Globe Scientific
Version/Model Number
2911
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
November 17, 2021
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
LIB
Product Code Name
Device, General Purpose, Microbiology, Diagnostic
Public Device Record Key
139c9670-7894-449e-b4ac-b85df5ab366a
Public Version Date
December 08, 2021
Public Version Number
4
DI Record Publish Date
November 26, 2019
Package DI Number
00840095604932
Quantity per Package
10
Contains DI Package
00840095604925
Package Discontinue Date
November 17, 2021
Package Status
Not 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 | 184 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 3 |