Duns Number:791619393
Device Description: XL INSULATED DILATORS
Catalog Number
-
Brand Name
TSI
Version/Model Number
ML-0440S
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
March 18, 2020
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
K140088
Product Code
PDQ
Product Code Name
Neurosurgical Nerve Locator
Public Device Record Key
28054295-ad0f-40c9-bb77-c03adb222e14
Public Version Date
March 19, 2020
Public Version Number
4
DI Record Publish Date
October 14, 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 |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 2398 |
2 | A medical device with a moderate to high risk that requires special controls. | 51 |