Duns Number:079840876
Device Description: Trial Rasp, 43mm x 30mm x 14mm, 10
Catalog Number
SR-0793-1410
Brand Name
Specials
Version/Model Number
SR-0793-1410
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
HTR
Product Code Name
RASP
Public Device Record Key
24d837cf-c176-4585-999d-5776b9d60c74
Public Version Date
June 10, 2022
Public Version Number
2
DI Record Publish Date
February 17, 2022
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 | 5602 |
2 | A medical device with a moderate to high risk that requires special controls. | 14020 |
U | Unclassified | 21 |