Duns Number:315018218
Device Description: Bottom, without base perforation, Standard 3/4, aluminium, silver, outer length: 470 mm, o Bottom, without base perforation, Standard 3/4, aluminium, silver, outer length: 470 mm, outer width: 274 mm, outer heigth: 187 mm,inner length: 421 mm, inner width: 258 mm, inner heigth: 160 mm
Catalog Number
JK744
Brand Name
AESCULAP
Version/Model Number
JK744
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)
-
Over the Counter (OTC)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
KCT
Product Code Name
Sterilization wrap containers, trays, cassettes & other accessories
Public Device Record Key
c886369d-ac66-446e-b843-0a8f16486968
Public Version Date
July 08, 2021
Public Version Number
5
DI Record Publish Date
September 23, 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 | 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 |