Duns Number:315018218
Device Description: CASPAR Nerve Root Retractor, 9 1/2", (240 mm), working length: , 3 1/2", (90 mm), bayonet- CASPAR Nerve Root Retractor, 9 1/2", (240 mm), working length: , 3 1/2", (90 mm), bayonet-shaped, blunt, width: 4 mm, non-sterile, reusable
Catalog Number
FF697R
Brand Name
AESCULAP
Version/Model Number
FF697R
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
90146aa6-2cfa-46c0-830e-4410d5dd05dc
Public Version Date
April 30, 2020
Public Version Number
1
DI Record Publish Date
April 22, 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 |