Duns Number:340306351
Device Description: SIRORETRO-SETconsists of:E27659250160 SIRORETRO KL PRODE27659250240 SIRORETRO KR PRODE2765 SIRORETRO-SETconsists of:E27659250160 SIRORETRO KL PRODE27659250240 SIRORETRO KR PRODE27659250320 SIRORETRO GL PRODE27659250400 SIRORETRO GR PROD
Catalog Number
-
Brand Name
SIRORETRO
Version/Model Number
5457929
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In HIBCC
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
ELC
Product Code Name
Scaler, Ultrasonic
Public Device Record Key
10227a29-f64c-433f-808b-29a285dad503
Public Version Date
May 17, 2022
Public Version Number
5
DI Record Publish Date
September 16, 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 | 235 |
2 | A medical device with a moderate to high risk that requires special controls. | 326 |