Duns Number:832696038
Device Description: Snowden-Pencer MIS REPLACEMENT PART DIAMOND-FLEX CAP, WHITE DIAMOND-FLEX RETRACTORS 5 PER Snowden-Pencer MIS REPLACEMENT PART DIAMOND-FLEX CAP, WHITE DIAMOND-FLEX RETRACTORS 5 PER PACKAGE (X 5)
Catalog Number
89-9482
Brand Name
Snowden-Pencer
Version/Model Number
89-9482
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
GCJ
Product Code Name
Laparoscope, general & plastic surgery
Public Device Record Key
5de8aec2-4a7a-4e3b-b490-582ee9f1939b
Public Version Date
March 31, 2022
Public Version Number
4
DI Record Publish Date
September 21, 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 | 8016 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 6223 |