Duns Number:315018218
Device Description: Tubing Clamp, straight, 8", (200 mm), heavy wedge jaw, fluted, serrated, non-sterile, reus Tubing Clamp, straight, 8", (200 mm), heavy wedge jaw, fluted, serrated, non-sterile, reusable
Catalog Number
AN913R
Brand Name
AESCULAP
Version/Model Number
AN913R
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
HXD
Product Code Name
CLAMP
Public Device Record Key
0e8a87c2-e324-4977-8a98-026b106337f8
Public Version Date
May 29, 2020
Public Version Number
1
DI Record Publish Date
May 21, 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 |