Duns Number:315018218
Device Description: Bottom, without base perforation, Standard 1/2, outer length: 300 mm, outer width: 274 mm, Bottom, without base perforation, Standard 1/2, outer length: 300 mm, outer width: 274 mm, outer heigth: 90 mm, inner length: 254 mm, inner width: 258 mm, inner heigth: 75 mm
Catalog Number
JK340
Brand Name
AESCULAP
Version/Model Number
JK340
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
FRG
Product Code Name
Wrap, sterilization
Public Device Record Key
daaf00d6-f486-4ca8-bf8d-b841b19d6554
Public Version Date
July 08, 2021
Public Version Number
6
DI Record Publish Date
May 19, 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 |