Duns Number:131747628
Device Description: BURR,ROUND,HL,RETRACT,8 FLUTE,5.0MMX18CM
Catalog Number
AR-6500RRBE
Brand Name
Arthrex®
Version/Model Number
AR-6500RRBE
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
Yes
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
GFF
Product Code Name
BUR, SURGICAL, GENERAL & PLASTIC SURGERY
Public Device Record Key
1f990d3d-b2b6-4d39-84bd-5c9a1360709e
Public Version Date
July 04, 2022
Public Version Number
4
DI Record Publish Date
August 03, 2018
Package DI Number
10888867258744
Quantity per Package
5
Contains DI Package
00888867258747
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Box
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 6506 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 3411 |
| 3 | A medical device with high risk that requires premarket approval | 1 |
| U | Unclassified | 2 |