Duns Number:177939027
Device Description: Mabis Stethoscope, Single Head, Red
Catalog Number
-
Brand Name
Mabis
Version/Model Number
10-428-080
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
July 31, 2019
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
Yes
Prescription Use (Rx)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
LDE
Product Code Name
Stethoscope, Manual
Public Device Record Key
f8e39bc9-df95-4512-8b5d-fe2941fd8c83
Public Version Date
March 19, 2021
Public Version Number
3
DI Record Publish Date
September 24, 2016
Package DI Number
30817357021708
Quantity per Package
20
Contains DI Package
10817357021704
Package Discontinue Date
March 19, 2021
Package Status
Not in Commercial Distribution
Package Type
Box
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 49 |
2 | A medical device with a moderate to high risk that requires special controls. | 178 |