Duns Number:149183167
Device Description: MEDIAL BLADE
Catalog Number
48760060
Brand Name
LITe PEDICLE BASED RETRACTOR
Version/Model Number
48760060
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
-
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
GAD
Product Code Name
RETRACTOR
Public Device Record Key
79f3b32e-387f-490a-af8d-0f0867f55bb5
Public Version Date
May 10, 2021
Public Version Number
2
DI Record Publish Date
November 25, 2019
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 | 2688 |
2 | A medical device with a moderate to high risk that requires special controls. | 5304 |
3 | A medical device with high risk that requires premarket approval | 86 |